728655
chr6:70925774:G>A
COL9A1
NM_078485:c.*826C>T
THREE_PRIME_EXON
Unknown significance
rs533440374
This variant is a VUS because it does not have enough information.
728656
chr6:70925791:C>T
COL9A1
NM_078485:c.*809G>A
THREE_PRIME_EXON
Unknown significance
rs557539788
This variant is a VUS because it does not have enough information.
728657
chr6:70925954:A>G
COL9A1
NM_078485:c.*646T>C
THREE_PRIME_EXON
Unknown significance
rs746120474
This variant is a VUS because it does not have enough information.
728658
chr6:70926001:T>C
COL9A1
NM_078485:c.*599A>G
THREE_PRIME_EXON
Unknown significance
rs551683531
This variant is a VUS because it does not have enough information.
728659
chr6:70926042:C>T
COL9A1
NM_078485:c.*558G>A
THREE_PRIME_EXON
Benign
rs373018250
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
0
1322
0
0
1006
0
0
694
0
0
1008
0
6
978
0.0061
6
5008
0.00119808
728660
chr6:70926050:A>C
COL9A1
NM_078485:c.*550T>G
THREE_PRIME_EXON
Unknown significance
rs560557089
This variant is a VUS because it does not have enough information.
1
1322
0.0008
0
1006
0
0
694
0
0
1008
0
0
978
0
1
5008
0.000199681
728661
chr6:70926059:G>A
COL9A1
NM_078485:c.*541C>T
THREE_PRIME_EXON
Unknown significance
rs191432958
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
0
694
0
2
1008
0.002
0
978
0
2
5008
0.000399361
728662
chr6:70926062:A>T
COL9A1
NM_078485:c.*538T>A
THREE_PRIME_EXON
Benign
rs55709776
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
8
1322
0.0061
0
1006
0
0
694
0
0
1008
0
0
978
0
8
5008
0.00159744
728663
chr6:70926070:C>T
COL9A1
NM_078485:c.*530G>A
THREE_PRIME_EXON
Unknown significance
rs570034842
This variant is a VUS because it does not have enough information.
728664
chr6:70926097:C>T
COL9A1
NM_078485:c.*503G>A
THREE_PRIME_EXON
Unknown significance
rs375176049
This variant is a VUS because it does not have enough information.
728665
chr6:70926126:T>C
COL9A1
NM_078485:c.*474A>G
THREE_PRIME_EXON
Unknown significance
rs780122438
This variant is a VUS because it does not have enough information.
728666
chr6:70926172:ATA>-
COL9A1
NM_078485:c.*428_*432delTAT
THREE_PRIME_EXON
Unknown significance
rs751855141
This variant is a VUS because it does not have enough information.
728667
chr6:70926175:A>G
COL9A1
NM_078485:c.*425T>C
THREE_PRIME_EXON
Unknown significance
rs749364459
This variant is a VUS because it does not have enough information.
728668
chr6:70926188:T>C
COL9A1
NM_078485:c.*412A>G
THREE_PRIME_EXON
Unknown significance
rs186882898
This variant is a VUS because it does not have enough information.
1
1322
0.0008
0
1006
0
0
694
0
0
1008
0
0
978
0
1
5008
0.000199681
728669
chr6:70926220:T>C
COL9A1
NM_078485:c.*380A>G
THREE_PRIME_EXON
Unknown significance
rs771960432
This variant is a VUS because it does not have enough information.
728670
chr6:70926225:C>T
COL9A1
NM_078485:c.*375G>A
THREE_PRIME_EXON
Unknown significance
rs531745614
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
0
694
0
0
1008
0
1
978
0.001
1
5008
0.000199681
728671
chr6:70926235:C>G
COL9A1
NM_078485:c.*365G>C
THREE_PRIME_EXON
Unknown significance
rs191406921
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
3
694
0.0043
0
1008
0
0
978
0
3
5008
0.000599042
728672
chr6:70926240:C>T
COL9A1
NM_078485:c.*360G>A
THREE_PRIME_EXON
Unknown significance
rs565189871
This variant is a VUS because it does not have enough information.
1
1322
0.0008
0
1006
0
2
694
0.0029
0
1008
0
0
978
0
3
5008
0.000599042
728673
chr6:70926334:A>G
COL9A1
NM_078485:c.*266T>C
THREE_PRIME_EXON
Benign
rs1064250
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
611
1322
0.4622
416
1006
0.4135
269
694
0.3876
269
1008
0.2669
417
978
0.4264
1982
5008
0.395767
728674
chr6:70926357:C>T
COL9A1
NM_078485:c.*243G>A
THREE_PRIME_EXON
Unknown significance
rs201244576
This variant is a VUS because it does not have enough information.
728675
chr6:70926358:->T
COL9A1
NM_078485:c.*242_*243insA
THREE_PRIME_EXON
Benign
rs555755721
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
277
1322
0.2095
236
1006
0.2346
242
694
0.3487
347
1008
0.3442
215
978
0.2198
1317
5008
0.262979
728676
chr6:70926358:->TT
COL9A1
NM_078485:c.*242_*243insAA
THREE_PRIME_EXON
Unknown significance
rs555755721
This variant is a VUS because it does not have enough information.
728677
chr6:70926361:->GG
COL9A1
NM_078485:c.*239_*240insCC
THREE_PRIME_EXON
Unknown significance
rs796116774
This variant is a VUS because it does not have enough information.
728678
chr6:70926371:A>G
COL9A1
NM_078485:c.*229T>C
THREE_PRIME_EXON
Benign
rs2459555
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
288
1322
0.2179
46
1006
0.0457
27
694
0.0389
7
1008
0.0069
61
978
0.0624
429
5008
0.0856629
728679
chr6:70926404:A>G
COL9A1
NM_078485:c.*196T>C
THREE_PRIME_EXON
Unknown significance
rs770787617
This variant is a VUS because it does not have enough information.
728680
chr6:70926426:A>G
COL9A1
NM_078485:c.*174T>C
THREE_PRIME_EXON
Unknown significance
rs776515044
This variant is a VUS because it does not have enough information.
728681
chr6:70926435:C>G
COL9A1
NM_078485:c.*165G>C
THREE_PRIME_EXON
Unknown significance
rs759272502
This variant is a VUS because it does not have enough information.
728682
chr6:70926443:T>C
COL9A1
NM_078485:c.*157A>G
THREE_PRIME_EXON
Unknown significance
rs567006253
This variant is a VUS because it does not have enough information.
2
1322
0.0015
0
1006
0
0
694
0
0
1008
0
0
978
0
2
5008
0.000399361
728683
chr6:70926511:C>T
COL9A1
NM_078485:c.*89G>A
THREE_PRIME_EXON
Unknown significance
rs373398023
This variant is a VUS because it does not have enough information.
728684
chr6:70926552:C>T
COL9A1
NM_078485:c.*48G>A
THREE_PRIME_EXON
Unknown significance
rs373931410
This variant is a VUS because it does not have enough information.
0
8600
0
1
4406
0.000226963
1
13006
0.0000768876
1
10132
0.0000986972
0
11398
0
0
8474
0
0
6532
0
0
65368
0
0
884
0
0
16280
0
1
119068
0.00000839856
728685
chr6:70926554:T>C
COL9A1
NM_078485:c.*46A>G
THREE_PRIME_EXON
Unknown significance
rs750975498
This variant is a VUS because it does not have enough information.
0
10132
0
0
11408
0
0
8480
0
0
6534
0
0
65424
0
0
888
0
1
16292
0.0000613798
1
119158
0.00000839222
728686
chr6:70926562:G>T
COL9A1
NM_078485:c.*38C>A
THREE_PRIME_EXON
Unknown significance
rs759522163
This variant is a VUS because it does not have enough information.
0
10134
0
0
11408
0
0
8490
0
0
6534
0
4
65458
0.0000611079
0
888
0
0
16306
0
4
119218
0.000033552
728687
chr6:70926563:C>T
COL9A1
NM_078485:c.*37G>A
THREE_PRIME_EXON
Unknown significance
rs535973057
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
0
694
0
0
1008
0
2
978
0.002
2
5008
0.000399361
0
10138
0
1
11406
0.0000876732
0
8486
0
2
6536
0.000305998
1
65468
0.0000152746
0
888
0
11
16300
0.000674847
15
119222
0.000125816
728688
chr6:70926564:G>A
COL9A1
NM_078485:c.*36C>T
THREE_PRIME_EXON
Unknown significance
rs6923452
This variant is a VUS because it does not have enough information.
3
8600
0.000348837
0
4406
0
3
13006
0.000230663
0
1322
0
1
1006
0.001
0
694
0
0
1008
0
0
978
0
1
5008
0.000199681
0
10146
0
0
11418
0
1
8496
0.000117702
0
6540
0
4
65492
0.0000610762
0
886
0
0
16310
0
5
119288
0.0000419154
728689
chr6:70926572:T>G
COL9A1
NM_078485:c.*28A>C
THREE_PRIME_EXON
Unknown significance
rs371413126
This variant is a VUS because it does not have enough information.
1
8600
0.000116279
0
4406
0
1
13006
0.0000768876
728690
chr6:70926574:CAGA>-
COL9A1
NM_078485:c.*26_*31delTCTG
THREE_PRIME_EXON
Unknown significance
rs779371541
This variant is a VUS because it does not have enough information.
728691
chr6:70926575:A>G
COL9A1
NM_078485:c.*25T>C
THREE_PRIME_EXON
Unknown significance
rs755948864
This variant is a VUS because it does not have enough information.
0
10192
0
2
11440
0.000174825
0
8514
0
0
6558
0
0
65734
0
0
890
0
0
16328
0
2
119656
0.0000167146
728692
chr6:70926588:G>A
COL9A1
NM_078485:c.*12C>T
THREE_PRIME_EXON
Unknown significance
rs778177942
This variant is a VUS because it does not have enough information.
0
10246
0
1
11470
0.000087184
0
8554
0
0
6566
0
2
66028
0.0000302902
0
896
0
0
16374
0
3
120134
0.0000249721
728693
chr6:70926605:G>A
COL9A1
NM_078485:p.Pro678Ser
NM_078485:c.2032C>T
EXON32
Likely benign
rs374561398
Pathogenicity is based on prediction data only. 2 out of 6 predictions were pathogenic.
0.045
N
0.0
D
0.005;0.008;0.005
B
0.141834
N
1
N;N;N
2.03
C
0
8600
0
1
4406
0.000226963
1
13006
0.0000768876
1
10282
0.0000972573
0
11522
0
1
8572
0.000116659
0
6590
0
0
66240
0
0
902
0
0
16448
0
2
120556
0.0000165898
728694
chr6:70926605:G>T
COL9A1
NM_078485:p.Pro678Thr
NM_078485:c.2032C>A
EXON32
Likely benign
rs374561398
Pathogenicity is based on prediction data only. 2 out of 6 predictions were pathogenic.
0.045
N
0.0
D
0.023;0.039;0.023
B
0.141834
N
1
N;N;N
2.03
C
1
10282
0.0000972573
0
11522
0
0
8572
0
0
6590
0
0
66240
0
0
902
0
0
16448
0
1
120556
0.0000082949
728695
chr6:70926612:C>T
COL9A1
NM_078485:p.Gly675Gly
NM_078485:c.2025G>A
EXON32
Unknown significance
rs373430094
This variant is a VUS because it does not have enough information.
0
8600
0
1
4406
0.000226963
1
13006
0.0000768876
4
10284
0.000388954
0
11534
0
0
8588
0
0
6594
0
0
66280
0
0
902
0
0
16472
0
4
120654
0.0000331527
728696
chr6:70926613:C>T
COL9A1
NM_078485:p.Gly675Glu
NM_078485:c.2024G>A
EXON32
Unknown significance
rs370064762
This variant is a VUS because it does not have enough information.
0.892
N
0.0
D
1.0
D
0
D
0.997299
D;D;D
5.87
C
0
8600
0
1
4406
0.000226963
1
13006
0.0000768876
728697
chr6:70926625:G>C
COL9A1
NM_078485:p.Ala671Gly
NM_078485:c.2012C>G
EXON32
Unknown significance
rs745872166
This variant is a VUS because it does not have enough information.
0.108
N
0.2;0.211
T
0.983;0.995;0.997
D
0.006579
N
0.977101
D;D;D
5.0
C
0
10286
0
0
11548
0
0
8598
0
0
6596
0
0
66328
0
0
900
0
1
16488
0.0000606502
1
120744
0.00000828199
728698
chr6:70926629:G>A
COL9A1
NM_078485:p.Arg670Stop
NM_078485:c.2008C>T
EXON32
Unknown significance
rs145221543
This variant is a VUS because it does not have enough information.
0.045
N
0.420448
N
1
D;D
4.98
C
0
8600
0
1
4406
0.000226963
1
13006
0.0000768876
1
10276
0.0000973141
0
11552
0
0
8602
0
0
6596
0
1
66336
0.0000150748
0
902
0
0
16498
0
2
120762
0.0000165615
728699
chr6:70926629:G>T
COL9A1
NM_078485:p.Arg670Arg
NM_078485:c.2008C>A
EXON32
Unknown significance
rs145221543
This variant is a VUS because it does not have enough information.
0
10276
0
0
11552
0
0
8602
0
0
6596
0
1
66336
0.0000150748
0
902
0
0
16498
0
1
120762
0.00000828075
728700
chr6:70926638:C>A
COL9A1
NM_078485:p.Ala667Ser
NM_078485:c.1999G>T
EXON32
Unknown significance
rs747451078
This variant is a VUS because it does not have enough information.
-0.008
N
0.37;0.132
T
0.836;0.204;0.007
P;B;B
0.000107
N
0.992378
D;D;D
4.99
C
0
10282
0
0
11554
0
0
8608
0
0
6600
0
0
66326
0
0
904
0
1
16502
0.0000605987
1
120776
0.00000827979
728701
chr6:70926639:C>T
COL9A1
NM_078485:p.Gln666Gln
NM_078485:c.1998G>A
EXON32
Unknown significance
rs376876121
This variant is a VUS because it does not have enough information.
1
8600
0.000116279
0
4406
0
1
13006
0.0000768876
0
10278
0
0
11556
0
0
8612
0
0
6600
0
1
66336
0.0000150748
0
904
0
0
16502
0
1
120788
0.00000827897
728702
chr6:70926641:G>T
COL9A1
NM_078485:p.Gln666Lys
NM_078485:c.1996C>A
EXON32
Unknown significance
rs772906014
This variant is a VUS because it does not have enough information.
0.998
C
0.024;0.015
D
0.997;0.977;0.969
D
0.000001
D
0.999784
D;D;D
5.87
C
728703
chr6:70926645:G>A
COL9A1
NM_078485:p.Thr664Thr
NM_078485:c.1992C>T
EXON32
Unknown significance
rs567606245
This variant is a VUS because it does not have enough information.
0
1322
0
1
1006
0.001
0
694
0
0
1008
0
0
978
0
1
5008
0.000199681
0
10274
0
0
11558
0
0
8612
0
0
6600
0
3
66322
0.0000452339
0
904
0
0
16502
0
3
120772
0.0000248402
728704
chr6:70926659:G>C
COL9A1
NM_078485:p.Pro660Ala
NM_078485:c.1978C>G
EXON32
Unknown significance
rs764914222
This variant is a VUS because it does not have enough information.
0.998
C
0.457;0.014
T;D
0.88;0.945;0.477
P
0.000001
D
0.999743
D;D;D
5.87
C
728705
chr6:70926671:C>T
COL9A1
NM_078485:p.Gly656Ser
NM_078485:c.1966G>A
EXON32
Unknown significance
rs770502831
This variant is a VUS because it does not have enough information.
0.892
N
0.0;0.036
D
1.0
D
0
D
0.999999
D;D;D
5.87
C
0
10256
0
0
11558
0
0
8614
0
1
6598
0.000151561
0
66278
0
0
904
0
0
16508
0
1
120716
0.00000828391
728706
chr6:70926672:G>A
COL9A1
NM_078485:p.Pro655Pro
NM_078485:c.1965C>T
EXON32
Unknown significance
rs370324739
This variant is a VUS because it does not have enough information.
0
8600
0
1
4406
0.000226963
1
13006
0.0000768876
728707
chr6:70926677:G>A
COL9A1
NM_078485:p.Leu654Phe
NM_078485:c.1960C>T
EXON32
Unknown significance
rs773938837
This variant is a VUS because it does not have enough information.
0.998
C
0.176;0.062
T
0.997;0.991;0.56
D;D;P
0.00452
N
0.937461
D;D;D
5.87
C
0
10254
0
0
11558
0
0
8614
0
0
6598
0
1
66234
0.000015098
0
904
0
0
16510
0
1
120672
0.00000828693
728708
chr6:70926682:G>C
COL9A1
NM_078485:p.Pro652Arg
NM_078485:c.1955C>G
EXON32
Unknown significance
rs758916884
This variant is a VUS because it does not have enough information.
0.998
C
0.953;0.328
T
0.992;0.985;0.782
D;D;P
0.014857
N
0.999975
D;D;D
5.87
C
0
10208
0
0
11554
0
1
8608
0.000116171
0
6592
0
0
66154
0
0
904
0
0
16510
0
1
120530
0.00000829669
728709
chr6:70926689:C>T
COL9A1
NM_078485:p.Gly650Arg
NM_078485:c.1948G>A
EXON32
Unknown significance
rs767536535
This variant is a VUS because it does not have enough information.
0.892
N
0.0
D
1.0
D
0
D
1
D;D;D
5.87
C
0
10198
0
0
11550
0
0
8612
0
0
6592
0
0
66114
0
0
904
0
1
16510
0.0000605694
1
120480
0.00000830013
728710
chr6:70926690:C>T
COL9A1
NM_078485:p.Pro649Pro
NM_078485:c.1947G>A
EXON32
Unknown significance
rs199845159
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
0
694
0
1
1008
0.001
0
978
0
1
5008
0.000199681
0
10194
0
0
11552
0
1
8608
0.000116171
0
6592
0
0
66074
0
0
902
0
0
16508
0
1
120430
0.00000830358
728711
chr6:70926691:G>A
COL9A1
NM_078485:p.Pro649Leu
NM_078485:c.1946C>T
EXON32
Unknown significance
rs760617713
This variant is a VUS because it does not have enough information.
0.998
C
0.012;0.006
D
1.0
D
0
D
1
D;D;D
5.87
C
728712
chr6:70926695:G>A
COL9A1
NM_078485:p.Pro648Ser
NM_078485:c.1942C>T
EXON32
Unknown significance
rs763970167
This variant is a VUS because it does not have enough information.
0.998
C
0.059;0.08
T
1.0
D
0
D
1
D;D;D
5.87
C
0
10184
0
0
11554
0
0
8610
0
0
6586
0
1
66096
0.0000151295
0
902
0
0
16510
0
1
120442
0.00000830275
728713
chr6:70926695:G>T
COL9A1
NM_078485:p.Pro648Thr
NM_078485:c.1942C>A
EXON32
Unknown significance
rs763970167
This variant is a VUS because it does not have enough information.
0.998
C
0.021;0.044
D
1.0
D
0
D
1
D;D;D
5.87
C
0
10184
0
0
11554
0
1
8610
0.000116144
0
6586
0
0
66096
0
0
902
0
0
16510
0
1
120442
0.00000830275
728714
chr6:70926697:C>A
COL9A1
NM_078485:p.Gly647Val
NM_078485:c.1940G>T
EXON32
Unknown significance
rs757561926
This variant is a VUS because it does not have enough information.
0.892
N
0.0
D
1.0
D
0
D
1
D;D;D
5.87
C
0
10164
0
0
11552
0
0
8606
0
0
6586
0
1
66028
0.0000151451
0
902
0
0
16510
0
1
120348
0.00000830924
728716
chr6:70926722:C>G
COL9A1
NM_078485:p.Val639Leu
NM_078485:c.1915G>C
EXON32
Likely benign
rs1056923
Pathogenicity is based on prediction data only. 2 out of 6 predictions were pathogenic.
0.042
N
0.402;0.626
T
0.888;0.798;0.296
P;P;B
0.006532
N
0.999953
N;N;N
1.79
C
728715
chr6:70926722:C>T
COL9A1
NM_078485:p.Val639Met
NM_078485:c.1915G>A
EXON32
Likely benign
rs1056923
Pathogenicity is based on prediction data only. 2 out of 6 predictions were pathogenic.
0.042
N
0.125;0.065
T
0.999;0.993;0.957
D
0.006532
N
0.999945
N;N;N
1.79
C
0
10068
0
0
11544
0
1
8598
0.000116306
0
6586
0
0
65780
0
0
900
0
0
16504
0
1
119980
0.00000833472
728717
chr6:70926729:G>A
COL9A1
NM_078485:p.Pro636Pro
NM_078485:c.1908C>T
EXON32
Unknown significance
rs750538159
This variant is a VUS because it does not have enough information.
0
10018
0
0
11540
0
0
8588
0
0
6586
0
3
65696
0.0000456649
0
896
0
0
16502
0
3
119826
0.0000250363
728718
chr6:70926737:G>C
COL9A1
NM_078485:p.Arg634Gly
NM_078485:c.1900C>G
EXON32
Unknown significance
rs758388716
This variant is a VUS because it does not have enough information.
0.998
C
0.014;0.087
D;T
0.995;0.98;0.351
D;D;B
0.000065
D
0.586536
N;N;N
4.98
C
0
9960
0
0
11534
0
0
8584
0
0
6580
0
0
65528
0
0
894
0
2
16498
0.000121227
2
119578
0.0000167255
728719
chr6:70926743:C>T
COL9A1
NM_078485:p.Gly632Ser
NM_078485:c.1894G>A
EXON32
Unknown significance
rs199581593
This variant is a VUS because it does not have enough information.
0.892
N
0.0
D
1.0
D
0
D
1
D;D;D
5.87
C
0
9904
0
0
11526
0
0
8578
0
1
6580
0.000151976
4
65342
0.0000612164
0
898
0
1
16496
0.0000606208
6
119324
0.0000502833
728721
chr6:70926744:G>A
COL9A1
NM_078485:p.Asp631Asp
NM_078485:c.1893C>T
EXON32
Unknown significance
rs149139869
This variant is a VUS because it does not have enough information.
3
8600
0.000348837
0
4406
0
3
13006
0.000230663
0
9902
0
0
11526
0
2
8582
0.000233046
0
6580
0
6
65338
0.0000918302
0
898
0
0
16496
0
8
119322
0.0000670455
728720
chr6:70926744:G>C
COL9A1
NM_078485:p.Asp631Glu
NM_078485:c.1893C>G
EXON32
Unknown significance
rs149139869
This variant is a VUS because it does not have enough information.
-1.648
N
0.165;0.015
T;D
1.0;1.0;0.999
D
0
D
0.999187
D;D;D
-3.09
N
0
9902
0
0
11526
0
1
8582
0.000116523
0
6580
0
0
65338
0
0
898
0
0
16496
0
1
119322
0.00000838068
728723
chr6:70926748:C>A
COL9A1
NM_078485:p.Arg630Leu
NM_078485:c.1889G>T
EXON32
Unknown significance
rs201520437
This variant is a VUS because it does not have enough information.
-1.007
N
0.007;0.244
D;T
0.999;0.998;0.999
D
0
D
0.999977
D;D;D
3.18
C
0
9878
0
0
11522
0
0
8580
0
0
6578
0
3
65320
0.0000459277
0
898
0
0
16494
0
3
119270
0.000025153
728722
chr6:70926748:C>T
COL9A1
NM_078485:p.Arg630Gln
NM_078485:c.1889G>A
EXON32
Unknown significance
rs201520437
This variant is a VUS because it does not have enough information.
-1.007
N
0.092;0.205
T
0.986;0.983;0.999
D
0
D
0.999826
D;D;D
3.18
C
0
1322
0
0
1006
0
0
694
0
1
1008
0.001
0
978
0
1
5008
0.000199681
0
9878
0
0
11522
0
0
8580
0
0
6578
0
1
65320
0.0000153092
0
898
0
0
16494
0
1
119270
0.00000838434
728724
chr6:70926749:G>C
COL9A1
NM_078485:p.Arg630Gly
NM_078485:c.1888C>G
EXON32
Unknown significance
rs200829297
This variant is a VUS because it does not have enough information.
0.998
C
0.005;0.068
D;T
1.0;0.998;0.999
D
0
D
0.999978
D;D;D
5.87
C
2
8600
0.000232558
0
4406
0
2
13006
0.000153775
0
9876
0
0
11522
0
0
8576
0
0
6576
0
2
65278
0.0000306382
0
898
0
0
16494
0
2
119220
0.0000167757
728725
chr6:70926753:A>G
COL9A1
NM_078485:p.Asn628Asn
NM_078485:c.1884T>C
EXON32
Unknown significance
rs773848465
This variant is a VUS because it does not have enough information.
0
9846
0
7
11518
0.000607744
0
8578
0
0
6576
0
0
65234
0
0
898
0
0
16494
0
7
119144
0.0000587524
728726
chr6:70926757:C>T
COL9A1
NM_078485:p.Arg627Lys
NM_078485:c.1880G>A
EXON32
Likely benign
rs1056921
Pathogenicity is based on prediction data only. 1 out of 6 predictions were pathogenic.
0.049
N
0.937;0.4
T
0.092;0.007;0.0
B
0.000433
N
0.614331
N;N;N
2.67
C
728727
chr6:70926759:G>C
COL9A1
NM_078485:p.Gly626Gly
NM_078485:c.1878C>G
EXON32
Unknown significance
rs1056920
This variant is a VUS because it does not have enough information.
728728
chr6:70926776:C>G
COL9A1
NM_078485:p.Gly621Arg
NM_078485:c.1861G>C
EXON32
Unknown significance
rs745421286
This variant is a VUS because it does not have enough information.
0.892
N
0.0
D
1.0
D
0
D
1
D;D;D
4.75
C
0
9622
0
1
11492
0.0000870171
0
8550
0
0
6558
0
0
64734
0
0
886
0
0
16472
0
1
118314
0.00000845209
728729
chr6:70926778:G>A
COL9A1
NM_078485:p.Pro620Leu
NM_078485:c.1859C>T
EXON32
Unknown significance
rs569046385
This variant is a VUS because it does not have enough information.
0.108
N
0.045;0.009
D
1.0
D
0.000026
D
1
D;D;D
4.76
C
728730
chr6:70926781:T>G
COL9A1
NM_078485:p.Asp619Ala
NM_078485:c.1856A>C
EXON32
Unknown significance
rs202176764
This variant is a VUS because it does not have enough information.
1.011
C
0.229;0.085
T
0.881;0.666;0.124
P;P;B
0.000001
D
0.998343
D;D;D
5.63
C
9
8596
0.001047
0
4406
0
9
13002
0.000692201
0
1322
0
1
1006
0.001
0
694
0
0
1008
0
0
978
0
1
5008
0.000199681
0
9612
0
0
11484
0
0
8552
0
0
6552
0
43
64704
0.000664565
0
886
0
0
16468
0
43
118258
0.000363612
728731
chr6:70926786:T>C
COL9A1
NM_078485:c.1853-2A>G
INTRON31
Unknown significance
rs775559838
This variant is a VUS because it does not have enough information.
1.011
C
1
D
5.63
C
0
9560
0
0
11476
0
0
8548
0
0
6548
0
0
64610
0
0
886
0
1
16464
0.0000607386
1
118092
0.00000846797
728732
chr6:70926787:G>A
COL9A1
NM_078485:c.1853-3C>T
INTRON31
Unknown significance
rs760704462
This variant is a VUS because it does not have enough information.
0
9528
0
1
11474
0.0000871536
0
8544
0
0
6548
0
1
64530
0.0000154967
0
882
0
0
16458
0
2
117964
0.0000169543
728733
chr6:70926790:AC>-
COL9A1
NM_078485:c.1853-6_1853-3delGT
INTRON31
Unknown significance
rs773034538
This variant is a VUS because it does not have enough information.
0
9538
0
0
11476
0
0
8544
0
0
6548
0
6
64526
0.0000929858
0
882
0
0
16460
0
6
117974
0.0000508587
728734
chr6:70926799:A>G
COL9A1
NM_078485:c.1853-15T>C
INTRON31
Unknown significance
rs764060012
This variant is a VUS because it does not have enough information.
0
9488
0
0
11466
0
0
8542
0
0
6548
0
0
64326
0
0
880
0
1
16442
0.0000608199
1
117692
0.00000849675
728735
chr6:70926805:C>T
COL9A1
NM_078485:c.1853-21G>A
INTRON31
Unknown significance
rs776603064
This variant is a VUS because it does not have enough information.
0
9440
0
0
11446
0
0
8532
0
0
6526
0
1
64196
0.0000155773
0
876
0
0
16434
0
1
117450
0.00000851426
728736
chr6:70926807:C>T
COL9A1
NM_078485:c.1853-23G>A
INTRON31
Unknown significance
rs761652460
This variant is a VUS because it does not have enough information.
0
9446
0
0
11442
0
0
8530
0
0
6532
0
1
64200
0.0000155763
0
876
0
1
16430
0.0000608643
2
117456
0.0000170277
728737
chr6:70926819:A>G
COL9A1
NM_078485:c.1853-35T>C
INTRON31
Unknown significance
rs765545489
This variant is a VUS because it does not have enough information.
0
9414
0
0
11418
0
2
8504
0.000235183
0
6516
0
0
64008
0
0
876
0
0
16414
0
2
117150
0.0000170721
728738
chr6:70926821:A>G
COL9A1
NM_078485:c.1853-37T>C
INTRON31
Unknown significance
rs750581928
This variant is a VUS because it does not have enough information.
0
9394
0
0
11404
0
0
8498
0
0
6500
0
1
63972
0.0000156318
0
874
0
0
16412
0
1
117054
0.00000854307
728739
chr6:70926823:T>C
COL9A1
NM_078485:c.1853-39A>G
INTRON31
Unknown significance
rs372462643
This variant is a VUS because it does not have enough information.
0
8590
0
1
4398
0.000227376
1
12988
0.0000769941
728740
chr6:70926824:C>A
COL9A1
NM_078485:c.1853-40G>T
INTRON31
Unknown significance
rs200640478
This variant is a VUS because it does not have enough information.
19
8590
0.00221187
1
4398
0.000227376
20
12988
0.00153988
0
1322
0
2
1006
0.002
1
694
0.0014
0
1008
0
1
978
0.001
4
5008
0.000798722
1
9388
0.000106519
25
11402
0.0021926
0
8488
0
1
6496
0.000153941
116
63898
0.00181539
2
876
0.00228311
55
16410
0.00335161
200
116958
0.00171002
728741
chr6:70926829:T>C
COL9A1
NM_078485:c.1853-45A>G
INTRON31
Unknown significance
rs370148201
This variant is a VUS because it does not have enough information.
1
8584
0.000116496
0
4398
0
1
12982
0.0000770297
0
9360
0
0
11392
0
0
8476
0
0
6494
0
6
63824
0.0000940085
0
876
0
1
16396
0.0000609905
7
116818
0.0000599223
728742
chr6:70926835:C>T
COL9A1
NM_078485:c.1853-51G>A
INTRON31
Unknown significance
rs373065340
This variant is a VUS because it does not have enough information.
1
8582
0.000116523
0
4396
0
1
12978
0.0000770535
0
9298
0
0
11336
0
0
8438
0
0
6446
0
1
63550
0.0000157356
0
868
0
0
16358
0
1
116294
0.0000085989
728743
chr6:70926854:G>A
COL9A1
NM_078485:c.1853-70C>T
INTRON31
Unknown significance
rs554434490
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
0
694
0
0
1008
0
1
978
0.001
1
5008
0.000199681
728744
chr6:70926863:C>T
COL9A1
NM_078485:c.1853-79G>A
INTRON31
Unknown significance
rs574305278
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
0
694
0
0
1008
0
1
978
0.001
1
5008
0.000199681
728745
chr6:70926887:C>T
COL9A1
NM_078485:c.1853-103G>A
INTRON31
Benign
rs9455004
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
79
1322
0.0598
1
1006
0.001
4
694
0.0058
0
1008
0
0
978
0
84
5008
0.0167732
728746
chr6:70926888:G>A
COL9A1
NM_078485:c.1853-104C>T
INTRON31
Unknown significance
rs778257967
This variant is a VUS because it does not have enough information.
728747
chr6:70926898:G>A
COL9A1
NM_078485:c.1853-114C>T
INTRON31
Benign
rs1200569
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
1124
1322
0.8502
733
1006
0.7286
597
694
0.8602
829
1008
0.8224
734
978
0.7505
4017
5008
0.802117
728748
chr6:70926933:G>C
COL9A1
NM_078485:c.1853-149C>G
INTRON31
Benign
rs2881343
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
374
1322
0.2829
156
1006
0.1551
149
694
0.2147
98
1008
0.0972
255
978
0.2607
1032
5008
0.20607
728749
chr6:70926941:T>C
COL9A1
NM_078485:c.1853-157A>G
INTRON31
Unknown significance
rs750731160
This variant is a VUS because it does not have enough information.
728750
chr6:70926948:A>G
COL9A1
NM_078485:c.1853-164T>C
INTRON31
Benign
rs9455005
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
79
1322
0.0598
1
1006
0.001
4
694
0.0058
1
1008
0.001
0
978
0
85
5008
0.0169728
728751
chr6:70926955:T>C
COL9A1
NM_078485:c.1853-171A>G
INTRON31
Unknown significance
rs565025254
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
1
694
0.0014
0
1008
0
0
978
0
1
5008
0.000199681
728752
chr6:70926979:A>G
COL9A1
NM_078485:c.1853-195T>C
INTRON31
Unknown significance
rs116353596
This variant is a VUS because it does not have enough information.
6
1322
0.0045
0
1006
0
0
694
0
0
1008
0
0
978
0
6
5008
0.00119808
728753
chr6:70927015:T>A
COL9A1
NM_078485:c.1853-231A>T
INTRON31
Benign
rs77849671
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
36
1322
0.0272
0
1006
0
2
694
0.0029
0
1008
0
0
978
0
38
5008
0.00758786
728754
chr6:70927022:C>T
COL9A1
NM_078485:c.1853-238G>A
INTRON31
Unknown significance
rs753964715
This variant is a VUS because it does not have enough information.
728755
chr6:70927042:C>T
COL9A1
NM_078485:c.1853-258G>A
INTRON31
Benign
rs182674097
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
17
1322
0.0129
0
1006
0
0
694
0
0
1008
0
0
978
0
17
5008
0.00339457
728756
chr6:70927127:A>C
COL9A1
NM_078485:c.1853-343T>G
INTRON31
Unknown significance
rs570598744
This variant is a VUS because it does not have enough information.
4
1322
0.003
0
1006
0
0
694
0
0
1008
0
0
978
0
4
5008
0.000798722
728757
chr6:70927152:G>C
COL9A1
NM_078485:c.1853-368C>G
INTRON31
Benign
rs662828
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
461
1322
0.3487
300
1006
0.2982
322
694
0.464
444
1008
0.4405
257
978
0.2628
1784
5008
0.35623
728758
chr6:70927154:T>C
COL9A1
NM_078485:c.1853-370A>G
INTRON31
Unknown significance
rs546784496
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
0
694
0
0
1008
0
1
978
0.001
1
5008
0.000199681
728759
chr6:70927185:T>G
COL9A1
NM_078485:c.1853-401A>C
INTRON31
Unknown significance
rs746988967
This variant is a VUS because it does not have enough information.
728760
chr6:70927220:C>T
COL9A1
NM_078485:c.1853-436G>A
INTRON31
Unknown significance
rs770715612
This variant is a VUS because it does not have enough information.
728761
chr6:70927268:T>A
COL9A1
NM_078485:c.1853-484A>T
INTRON31
Unknown significance
rs112749797
This variant is a VUS because it does not have enough information.
728762
chr6:70927290:G>T
COL9A1
NM_078485:c.1853-506C>A
INTRON31
Unknown significance
rs377694621
This variant is a VUS because it does not have enough information.
728763
chr6:70927312:A>G
COL9A1
NM_078485:c.1853-528T>C
INTRON31
Unknown significance
rs558058201
This variant is a VUS because it does not have enough information.
0
1322
0
1
1006
0.001
2
694
0.0029
0
1008
0
1
978
0.001
4
5008
0.000798722
728764
chr6:70927330:G>A
COL9A1
NM_078485:c.1853-546C>T
INTRON31
Benign
rs9455006
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
79
1322
0.0598
1
1006
0.001
4
694
0.0058
0
1008
0
0
978
0
84
5008
0.0167732
728765
chr6:70927331:C>A
COL9A1
NM_078485:c.1853-547G>T
INTRON31
Unknown significance
rs568856737
This variant is a VUS because it does not have enough information.
728766
chr6:70927333:C>T
COL9A1
NM_078485:c.1853-549G>A
INTRON31
Unknown significance
rs571945044
This variant is a VUS because it does not have enough information.
1
1322
0.0008
0
1006
0
0
694
0
0
1008
0
0
978
0
1
5008
0.000199681
728767
chr6:70927384:T>C
COL9A1
NM_078485:c.1853-600A>G
INTRON31
Unknown significance
rs534467225
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
0
694
0
1
1008
0.001
0
978
0
1
5008
0.000199681
728768
chr6:70927392:C>T
COL9A1
NM_078485:c.1853-608G>A
INTRON31
Unknown significance
rs576424152
This variant is a VUS because it does not have enough information.
728769
chr6:70927397:G>A
COL9A1
NM_078485:c.1853-613C>T
INTRON31
Unknown significance
rs543603395
This variant is a VUS because it does not have enough information.
728770
chr6:70927415:T>C
COL9A1
NM_078485:c.1853-631A>G
INTRON31
Unknown significance
rs150392551
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
0
694
0
2
1008
0.002
0
978
0
2
5008
0.000399361
728771
chr6:70927425:A>C
COL9A1
NM_078485:c.1853-641T>G
INTRON31
Unknown significance
rs769333464
This variant is a VUS because it does not have enough information.
728772
chr6:70927434:G>A
COL9A1
NM_078485:c.1853-650C>T
INTRON31
Benign
rs661521
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
288
1322
0.2179
47
1006
0.0467
27
694
0.0389
7
1008
0.0069
61
978
0.0624
430
5008
0.0858626
728773
chr6:70927508:T>A
COL9A1
NM_078485:c.1853-724A>T
INTRON31
Benign
rs1200568
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
386
1322
0.292
299
1006
0.2972
318
694
0.4582
444
1008
0.4405
257
978
0.2628
1704
5008
0.340256
728774
chr6:70927523:C>T
COL9A1
NM_078485:c.1853-739G>A
INTRON31
Unknown significance
rs762410593
This variant is a VUS because it does not have enough information.
728775
chr6:70927531:T>C
COL9A1
NM_078485:c.1853-747A>G
INTRON31
Unknown significance
rs556380808
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
0
694
0
0
1008
0
2
978
0.002
2
5008
0.000399361
728776
chr6:70927666:->A
COL9A1
NM_078485:c.1853-882_1853-881insT
INTRON31
Unknown significance
rs541153953
This variant is a VUS because it does not have enough information.
728777
chr6:70927672:C>T
COL9A1
NM_078485:c.1853-888G>A
INTRON31
Unknown significance
rs768672054
This variant is a VUS because it does not have enough information.
728778
chr6:70927687:T>C
COL9A1
NM_078485:c.1853-903A>G
INTRON31
Unknown significance
rs576521971
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
0
694
0
0
1008
0
1
978
0.001
1
5008
0.000199681
728779
chr6:70927752:A>G
COL9A1
NM_078485:c.1853-968T>C
INTRON31
Unknown significance
rs545059587
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
0
694
0
1
1008
0.001
0
978
0
1
5008
0.000199681
728780
chr6:70927754:G>A
COL9A1
NM_078485:c.1853-970C>T
INTRON31
Benign
rs138158570
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
45
1322
0.034
0
1006
0
1
694
0.0014
0
1008
0
0
978
0
46
5008
0.0091853
728781
chr6:70927771:G>A
COL9A1
NM_078485:c.1853-987C>T
INTRON31
Unknown significance
rs761675420
This variant is a VUS because it does not have enough information.
728782
chr6:70927789:T>C
COL9A1
NM_078485:c.1853-1005A>G
INTRON31
Benign
rs142404885
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
31
1322
0.0234
0
1006
0
2
694
0.0029
0
1008
0
0
978
0
33
5008
0.00658946
728783
chr6:70927825:G>A
COL9A1
NM_078485:c.1853-1041C>T
INTRON31
Unknown significance
rs540895476
This variant is a VUS because it does not have enough information.
0
1322
0
1
1006
0.001
0
694
0
0
1008
0
0
978
0
1
5008
0.000199681
728784
chr6:70927840:C>T
COL9A1
NM_078485:c.1853-1056G>A
INTRON31
Unknown significance
rs779580023
This variant is a VUS because it does not have enough information.
728785
chr6:70927841:G>C
COL9A1
NM_078485:c.1853-1057C>G
INTRON31
Unknown significance
rs560859980
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
1
694
0.0014
0
1008
0
0
978
0
1
5008
0.000199681
728786
chr6:70927844:T>A
COL9A1
NM_078485:c.1853-1060A>T
INTRON31
Unknown significance
rs763042157
This variant is a VUS because it does not have enough information.
728787
chr6:70927849:->AAT
COL9A1
NM_078485:c.1853-1065_1853-1064insATT
INTRON31
Benign
rs557920792
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
8
1322
0.0061
0
1006
0
0
694
0
0
1008
0
1
978
0.001
9
5008
0.00179712
728788
chr6:70927881:C>T
COL9A1
NM_078485:c.1853-1097G>A
INTRON31
Unknown significance
rs773688963
This variant is a VUS because it does not have enough information.
728789
chr6:70927886:G>A
COL9A1
NM_078485:c.1853-1102C>T
INTRON31
Unknown significance
rs184914476
This variant is a VUS because it does not have enough information.
0
1322
0
2
1006
0.002
0
694
0
0
1008
0
0
978
0
2
5008
0.000399361
728790
chr6:70927904:T>C
COL9A1
NM_078485:c.1853-1120A>G
INTRON31
Unknown significance
rs767948610
This variant is a VUS because it does not have enough information.
728791
chr6:70927910:T>C
COL9A1
NM_078485:c.1853-1126A>G
INTRON31
Unknown significance
rs146611546
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
0
694
0
1
1008
0.001
0
978
0
1
5008
0.000199681
728792
chr6:70927937:T>C
COL9A1
NM_078485:c.1853-1153A>G
INTRON31
Unknown significance
rs563219814
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
0
694
0
0
1008
0
1
978
0.001
1
5008
0.000199681
728793
chr6:70927944:G>C
COL9A1
NM_078485:c.1853-1160C>G
INTRON31
Unknown significance
rs532911506
This variant is a VUS because it does not have enough information.
728794
chr6:70927967:T>A
COL9A1
NM_078485:c.1853-1183A>T
INTRON31
Benign
rs476863
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
460
1322
0.348
300
1006
0.2982
322
694
0.464
444
1008
0.4405
257
978
0.2628
1783
5008
0.35603
728795
chr6:70927975:T>C
COL9A1
NM_078485:c.1853-1191A>G
INTRON31
Unknown significance
rs552007772
This variant is a VUS because it does not have enough information.
1
1322
0.0008
0
1006
0
0
694
0
0
1008
0
0
978
0
1
5008
0.000199681
728796
chr6:70928002:A>G
COL9A1
NM_078485:c.1853-1218T>C
INTRON31
Unknown significance
rs565644726
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
1
694
0.0014
0
1008
0
0
978
0
1
5008
0.000199681
728797
chr6:70928009:T>G
COL9A1
NM_078485:c.1853-1225A>C
INTRON31
Unknown significance
rs528101602
This variant is a VUS because it does not have enough information.
1
1322
0.0008
0
1006
0
0
694
0
0
1008
0
0
978
0
1
5008
0.000199681
728798
chr6:70928032:G>A
COL9A1
NM_078485:c.1853-1248C>T
INTRON31
Unknown significance
rs548062553
This variant is a VUS because it does not have enough information.
1
1322
0.0008
0
1006
0
1
694
0.0014
0
1008
0
0
978
0
2
5008
0.000399361
728799
chr6:70928042:G>T
COL9A1
NM_078485:c.1853-1258C>A
INTRON31
Unknown significance
rs766625505
This variant is a VUS because it does not have enough information.
728800
chr6:70928046:G>A
COL9A1
NM_078485:c.1853-1262C>T
INTRON31
Unknown significance
rs754117076
This variant is a VUS because it does not have enough information.
728801
chr6:70928060:G>A
COL9A1
NM_078485:c.1853-1276C>T
INTRON31
Unknown significance
rs755105909
This variant is a VUS because it does not have enough information.
728802
chr6:70928077:G>A
COL9A1
NM_078485:c.1853-1293C>T
INTRON31
Unknown significance
rs568008085
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
0
694
0
1
1008
0.001
0
978
0
1
5008
0.000199681
728803
chr6:70928089:G>A
COL9A1
NM_078485:c.1853-1305C>T
INTRON31
Benign
rs370453291
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
0
1322
0
0
1006
0
0
694
0
0
1008
0
15
978
0.0153
15
5008
0.00299521
728804
chr6:70928091:G>A
COL9A1
NM_078485:c.1853-1307C>T
INTRON31
Unknown significance
rs189729053
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
0
694
0
1
1008
0.001
0
978
0
1
5008
0.000199681
728805
chr6:70928114:C>T
COL9A1
NM_078485:c.1853-1330G>A
INTRON31
Unknown significance
rs779062530
This variant is a VUS because it does not have enough information.
728806
chr6:70928152:C>T
COL9A1
NM_078485:c.1853-1368G>A
INTRON31
Unknown significance
rs570029367
This variant is a VUS because it does not have enough information.
0
1322
0
1
1006
0.001
0
694
0
0
1008
0
0
978
0
1
5008
0.000199681
728807
chr6:70928195:G>C
COL9A1
NM_078485:c.1853-1411C>G
INTRON31
Unknown significance
rs759738915
This variant is a VUS because it does not have enough information.
728808
chr6:70928251:T>C
COL9A1
NM_078485:c.1853-1467A>G
INTRON31
Unknown significance
rs757284588
This variant is a VUS because it does not have enough information.
728809
chr6:70928322:T>C
COL9A1
NM_078485:c.1853-1538A>G
INTRON31
Unknown significance
rs183148585
This variant is a VUS because it does not have enough information.
0
1322
0
1
1006
0.001
0
694
0
0
1008
0
0
978
0
1
5008
0.000199681
728810
chr6:70928334:T>C
COL9A1
NM_078485:c.1853-1550A>G
INTRON31
Benign
rs72918976
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
2
1322
0.0015
9
1006
0.0089
2
694
0.0029
0
1008
0
3
978
0.0031
16
5008
0.00319489
728811
chr6:70928337:G>T
COL9A1
NM_078485:c.1853-1553C>A
INTRON31
Unknown significance
rs189118219
This variant is a VUS because it does not have enough information.
0
1322
0
1
1006
0.001
0
694
0
0
1008
0
0
978
0
1
5008
0.000199681
728812
chr6:70928359:T>C
COL9A1
NM_078485:c.1853-1575A>G
INTRON31
Unknown significance
rs758506278
This variant is a VUS because it does not have enough information.
728813
chr6:70928368:CTTTT>-
COL9A1
NM_078485:c.1853-1584_1853-1578delAAAAG
INTRON31
Unknown significance
rs372428882
This variant is a VUS because it does not have enough information.
728814
chr6:70928371:T>C
COL9A1
NM_078485:c.1853-1587A>G
INTRON31
Benign
rs541032331
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
8
1322
0.0061
0
1006
0
1
694
0.0014
0
1008
0
0
978
0
9
5008
0.00179712
728815
chr6:70928392:C>-
COL9A1
NM_078485:c.1853-1608delG
INTRON31
Unknown significance
rs373177713
This variant is a VUS because it does not have enough information.
728816
chr6:70928392:C>T
COL9A1
NM_078485:c.1853-1608G>A
INTRON31
Benign
rs12201251
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
75
1322
0.0567
252
1006
0.2505
291
694
0.4193
437
1008
0.4335
196
978
0.2004
1251
5008
0.2498
728817
chr6:70928398:A>T
COL9A1
NM_078485:c.1853-1614T>A
INTRON31
Unknown significance
rs778205161
This variant is a VUS because it does not have enough information.
728818
chr6:70928400:A>T
COL9A1
NM_078485:c.1853-1616T>A
INTRON31
Unknown significance
rs752112221
This variant is a VUS because it does not have enough information.
728819
chr6:70928402:G>T
COL9A1
NM_078485:c.1853-1618C>A
INTRON31
Unknown significance
rs757612482
This variant is a VUS because it does not have enough information.
728820
chr6:70928404:C>T
COL9A1
NM_078485:c.1853-1620G>A
INTRON31
Unknown significance
rs781466206
This variant is a VUS because it does not have enough information.
728821
chr6:70928431:G>T
COL9A1
NM_078485:c.1853-1647C>A
INTRON31
Unknown significance
rs549163102
This variant is a VUS because it does not have enough information.
0
1322
0
1
1006
0.001
0
694
0
0
1008
0
0
978
0
1
5008
0.000199681
728822
chr6:70928441:->AGTGGTCTT
COL9A1
NM_078485:c.1853-1657_1853-1656insAAGACCACT
INTRON31
Unknown significance
rs202152808
This variant is a VUS because it does not have enough information.
728823
chr6:70928441:->AGTGGTCTTATT
COL9A1
NM_078485:c.1853-1657_1853-1656insAATAAGACCACT
INTRON31
Unknown significance
rs202152808
This variant is a VUS because it does not have enough information.
728824
chr6:70928442:->G
COL9A1
NM_078485:c.1853-1658_1853-1657insC
INTRON31
Unknown significance
rs765711033
This variant is a VUS because it does not have enough information.
728825
chr6:70928442:T>C
COL9A1
NM_078485:c.1853-1658A>G
INTRON31
Unknown significance
rs16868762
This variant is a VUS because it does not have enough information.
728827
chr6:70928443:->AGGTCTTATTAC
COL9A1
NM_078485:c.1853-1659_1853-1658insGTAATAAGACCT
INTRON31
Unknown significance
rs3842608
This variant is a VUS because it does not have enough information.
728828
chr6:70928443:->GGTCTTATTAC
COL9A1
NM_078485:c.1853-1659_1853-1658insGTAATAAGACC
INTRON31
Unknown significance
rs66525752
This variant is a VUS because it does not have enough information.
728826
chr6:70928443:->GTGGTCTTATTAC
COL9A1
NM_078485:c.1853-1659_1853-1658insGTAATAAGACCAC
INTRON31
Unknown significance
rs369801517
This variant is a VUS because it does not have enough information.
728829
chr6:70928443:->TGGTCTTATTAC
COL9A1
NM_078485:c.1853-1659_1853-1658insGTAATAAGACCA
INTRON31
Unknown significance
rs66525752
This variant is a VUS because it does not have enough information.
728830
chr6:70928505:T>C
COL9A1
NM_078485:c.1853-1721A>G
INTRON31
Benign
rs491690
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
300
1322
0.2269
0
1006
0
13
694
0.0187
0
1008
0
0
978
0
313
5008
0.0625
728831
chr6:70928505:TT>CA
COL9A1
Unknown significance
rs386702482
This variant is a VUS because it does not have enough information.
728832
chr6:70928506:T>A
COL9A1
NM_078485:c.1853-1722A>T
INTRON31
Benign
rs75370620
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
98
1322
0.0741
0
1006
0
1
694
0.0014
0
1008
0
0
978
0
99
5008
0.0197684
728833
chr6:70928528:C>G
COL9A1
NM_078485:c.1853-1744G>C
INTRON31
Unknown significance
rs371962151
This variant is a VUS because it does not have enough information.
728834
chr6:70928600:A>G
COL9A1
NM_078485:c.1853-1816T>C
INTRON31
Benign
rs12333183
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
50
1322
0.0378
1
1006
0.001
2
694
0.0029
0
1008
0
0
978
0
53
5008
0.0105831
728835
chr6:70928628:G>C
COL9A1
NM_078485:c.1853-1844C>G
INTRON31
Unknown significance
rs567891451
This variant is a VUS because it does not have enough information.
728836
chr6:70928678:C>A
COL9A1
NM_078485:c.1853-1894G>T
INTRON31
Unknown significance
rs768138513
This variant is a VUS because it does not have enough information.
728837
chr6:70928686:G>A
COL9A1
NM_078485:c.1853-1902C>T
INTRON31
Unknown significance
rs545874453
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
0
694
0
0
1008
0
3
978
0.0031
3
5008
0.000599042
728838
chr6:70928699:C>G
COL9A1
NM_078485:c.1853-1915G>C
INTRON31
Unknown significance
rs779784277
This variant is a VUS because it does not have enough information.
728839
chr6:70928708:T>C
COL9A1
NM_078485:c.1853-1924A>G
INTRON31
Unknown significance
rs559493098
This variant is a VUS because it does not have enough information.
1
1322
0.0008
0
1006
0
0
694
0
0
1008
0
0
978
0
1
5008
0.000199681
728840
chr6:70928816:A>G
COL9A1
NM_078485:c.1853-2032T>C
INTRON31
Unknown significance
rs542932446
This variant is a VUS because it does not have enough information.
2
1322
0.0015
0
1006
0
0
694
0
0
1008
0
0
978
0
2
5008
0.000399361
728841
chr6:70928828:G>A
COL9A1
NM_078485:c.1853-2044C>T
INTRON31
Unknown significance
rs548249586
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
0
694
0
0
1008
0
1
978
0.001
1
5008
0.000199681
728842
chr6:70928844:A>G
COL9A1
NM_078485:c.1853-2060T>C
INTRON31
Benign
rs9346372
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
75
1322
0.0567
252
1006
0.2505
291
694
0.4193
438
1008
0.4345
196
978
0.2004
1252
5008
0.25
728843
chr6:70928882:C>T
COL9A1
NM_078485:c.1853-2098G>A
INTRON31
Unknown significance
rs73749904
This variant is a VUS because it does not have enough information.
1
1322
0.0008
0
1006
0
0
694
0
0
1008
0
1
978
0.001
2
5008
0.000399361
728844
chr6:70928883:G>A
COL9A1
NM_078485:c.1853-2099C>T
INTRON31
Benign
rs17691623
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
2
1322
0.0015
11
1006
0.0109
2
694
0.0029
14
1008
0.0139
0
978
0
29
5008
0.00579073
728845
chr6:70928914:C>A
COL9A1
NM_078485:c.1853-2130G>T
INTRON31
Benign
rs487928
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
301
1322
0.2277
47
1006
0.0467
27
694
0.0389
7
1008
0.0069
61
978
0.0624
443
5008
0.0884585
728846
chr6:70928914:C>G
COL9A1
NM_078485:c.1853-2130G>C
INTRON31
Unknown significance
rs487928
This variant is a VUS because it does not have enough information.
728847
chr6:70928998:G>-
COL9A1
NM_078485:c.1853-2214delC
INTRON31
Benign
rs562620805
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
30
1322
0.0227
0
1006
0
1
694
0.0014
0
1008
0
0
978
0
31
5008
0.0061901
728848
chr6:70929004:->A
COL9A1
NM_078485:c.1853-2220_1853-2219insT
INTRON31
Benign
rs148826101
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
3
1322
0.0023
32
1006
0.0318
6
694
0.0086
0
1008
0
11
978
0.0112
52
5008
0.0103834
728849
chr6:70929017:G>A
COL9A1
NM_078485:c.1853-2233C>T
INTRON31
Unknown significance
rs771982291
This variant is a VUS because it does not have enough information.
728850
chr6:70929020:A>T
COL9A1
NM_078485:c.1853-2236T>A
INTRON31
Unknown significance
rs761127709
This variant is a VUS because it does not have enough information.
728851
chr6:70929071:G>A
COL9A1
NM_078485:c.1853-2287C>T
INTRON31
Unknown significance
rs766748350
This variant is a VUS because it does not have enough information.
728852
chr6:70929088:C>G
COL9A1
NM_078485:c.1853-2304G>C
INTRON31
Unknown significance
rs538871527
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
1
694
0.0014
0
1008
0
0
978
0
1
5008
0.000199681
728853
chr6:70929089:G>A
COL9A1
NM_078485:c.1853-2305C>T
INTRON31
Unknown significance
rs754093013
This variant is a VUS because it does not have enough information.
728854
chr6:70929099:A>C
COL9A1
NM_078485:c.1853-2315T>G
INTRON31
Unknown significance
rs552208407
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
0
694
0
1
1008
0.001
0
978
0
1
5008
0.000199681
728855
chr6:70929132:G>A
COL9A1
NM_078485:c.1853-2348C>T
INTRON31
Unknown significance
rs565884793
This variant is a VUS because it does not have enough information.
0
1322
0
1
1006
0.001
0
694
0
0
1008
0
0
978
0
1
5008
0.000199681
728856
chr6:70929138:G>A
COL9A1
NM_078485:c.1853-2354C>T
INTRON31
Unknown significance
rs534681574
This variant is a VUS because it does not have enough information.
1
1322
0.0008
0
1006
0
0
694
0
0
1008
0
0
978
0
1
5008
0.000199681
728857
chr6:70929167:C>T
COL9A1
NM_078485:c.1853-2383G>A
INTRON31
Unknown significance
rs193135193
This variant is a VUS because it does not have enough information.
0
1322
0
2
1006
0.002
0
694
0
0
1008
0
0
978
0
2
5008
0.000399361
728858
chr6:70929213:C>T
COL9A1
NM_078485:c.1853-2429G>A
INTRON31
Unknown significance
rs765371389
This variant is a VUS because it does not have enough information.
728859
chr6:70929217:A>G
COL9A1
NM_078485:c.1853-2433T>C
INTRON31
Unknown significance
rs183587563
This variant is a VUS because it does not have enough information.
1
1322
0.0008
0
1006
0
0
694
0
0
1008
0
0
978
0
1
5008
0.000199681
728860
chr6:70929254:C>T
COL9A1
NM_078485:c.1853-2470G>A
INTRON31
Unknown significance
rs200327588
This variant is a VUS because it does not have enough information.
728861
chr6:70929277:C>T
COL9A1
NM_078485:c.1853-2493G>A
INTRON31
Unknown significance
rs537316187
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
0
694
0
0
1008
0
1
978
0.001
1
5008
0.000199681
728862
chr6:70929282:A>C
COL9A1
NM_078485:c.1853-2498T>G
INTRON31
Benign
rs188572138
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
0
1322
0
5
1006
0.005
0
694
0
0
1008
0
1
978
0.001
6
5008
0.00119808
728863
chr6:70929292:C>G
COL9A1
NM_078485:c.1853-2508G>C
INTRON31
Unknown significance
rs758531656
This variant is a VUS because it does not have enough information.
728865
chr6:70929296:G>C
COL9A1
NM_078485:c.1853-2512C>G
INTRON31
Unknown significance
rs191756110
This variant is a VUS because it does not have enough information.
728864
chr6:70929296:G>T
COL9A1
NM_078485:c.1853-2512C>A
INTRON31
Unknown significance
rs191756110
This variant is a VUS because it does not have enough information.
0
1322
0
1
1006
0.001
1
694
0.0014
0
1008
0
0
978
0
2
5008
0.000399361
728866
chr6:70929319:C>T
COL9A1
NM_078485:c.1853-2535G>A
INTRON31
Unknown significance
rs184182028
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
0
694
0
1
1008
0.001
0
978
0
1
5008
0.000199681
728867
chr6:70929327:T>C
COL9A1
NM_078485:c.1853-2543A>G
INTRON31
Unknown significance
rs760527581
This variant is a VUS because it does not have enough information.
728868
chr6:70929334:G>T
COL9A1
NM_078485:c.1853-2550C>A
INTRON31
Unknown significance
rs188166413
This variant is a VUS because it does not have enough information.
1
1322
0.0008
3
1006
0.003
2
694
0.0029
0
1008
0
1
978
0.001
7
5008
0.00139776
728869
chr6:70929368:G>A
COL9A1
NM_078485:c.1853-2584C>T
INTRON31
Unknown significance
rs796160588
This variant is a VUS because it does not have enough information.
728870
chr6:70929369:A>C
COL9A1
NM_078485:c.1853-2585T>G
INTRON31
Unknown significance
rs537381432
This variant is a VUS because it does not have enough information.
728871
chr6:70929411:C>T
COL9A1
NM_078485:c.1853-2627G>A
INTRON31
Benign
rs35022420
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
367
1322
0.2776
101
1006
0.1004
136
694
0.196
96
1008
0.0952
222
978
0.227
922
5008
0.184105
728872
chr6:70929411:CA>TG
COL9A1
Unknown significance
rs386702483
This variant is a VUS because it does not have enough information.
728873
chr6:70929412:A>G
COL9A1
NM_078485:c.1853-2628T>C
INTRON31
Benign
rs572716
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
1109
1322
0.8389
715
1006
0.7107
594
694
0.8559
713
1008
0.7073
675
978
0.6902
3806
5008
0.759984
728874
chr6:70929415:G>A
COL9A1
NM_078485:c.1853-2631C>T
INTRON31
Unknown significance
rs561697786
This variant is a VUS because it does not have enough information.
0
1322
0
2
1006
0.002
0
694
0
0
1008
0
0
978
0
2
5008
0.000399361
728875
chr6:70929463:G>T
COL9A1
NM_078485:c.1853-2679C>A
INTRON31
Unknown significance
rs754729533
This variant is a VUS because it does not have enough information.
728876
chr6:70929470:A>-
COL9A1
NM_078485:c.1853-2686delT
INTRON31
Benign
rs564251786
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
12
1322
0.0091
1
1006
0.001
0
694
0
0
1008
0
0
978
0
13
5008
0.00259585
728877
chr6:70929491:A>G
COL9A1
NM_078485:c.1853-2707T>C
INTRON31
Unknown significance
rs778405664
This variant is a VUS because it does not have enough information.
728878
chr6:70929514:C>G
COL9A1
NM_078485:c.1853-2730G>C
INTRON31
Unknown significance
rs747731798
This variant is a VUS because it does not have enough information.
728879
chr6:70929522:T>G
COL9A1
NM_078485:c.1853-2738A>C
INTRON31
Benign
rs10806630
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
7
1322
0.0053
100
1006
0.0994
23
694
0.0331
33
1008
0.0327
100
978
0.1022
263
5008
0.052516
728880
chr6:70929526:A>T
COL9A1
NM_078485:c.1853-2742T>A
INTRON31
Unknown significance
rs550412692
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
0
694
0
0
1008
0
1
978
0.001
1
5008
0.000199681
728881
chr6:70929527:T>-
COL9A1
NM_078485:c.1853-2743delA
INTRON31
Benign
rs552997977
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
0
1322
0
7
1006
0.007
1
694
0.0014
0
1008
0
0
978
0
8
5008
0.00159744
728882
chr6:70929597:A>G
COL9A1
NM_078485:c.1853-2813T>C
INTRON31
Unknown significance
rs546645983
This variant is a VUS because it does not have enough information.
728883
chr6:70929616:A>G
COL9A1
NM_078485:c.1853-2832T>C
INTRON31
Benign
rs563832286
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
9
1322
0.0068
0
1006
0
1
694
0.0014
0
1008
0
0
978
0
10
5008
0.00199681
728884
chr6:70929621:T>-
COL9A1
NM_078485:c.1853-2837delA
INTRON31
Unknown significance
rs35130017
This variant is a VUS because it does not have enough information.
728885
chr6:70929715:C>A
COL9A1
NM_078485:c.1853-2931G>T
INTRON31
Unknown significance
rs532738653
This variant is a VUS because it does not have enough information.
1
1322
0.0008
0
1006
0
0
694
0
0
1008
0
0
978
0
1
5008
0.000199681
728886
chr6:70929758:C>T
COL9A1
NM_078485:c.1853-2974G>A
INTRON31
Unknown significance
rs191479699
This variant is a VUS because it does not have enough information.
5
1322
0.0038
0
1006
0
1
694
0.0014
0
1008
0
0
978
0
6
5008
0.00119808
728887
chr6:70929814:C>A
COL9A1
NM_078485:c.1853-3030G>T
INTRON31
Unknown significance
rs747528454
This variant is a VUS because it does not have enough information.
728888
chr6:70929834:T>C
COL9A1
NM_078485:c.1853-3050A>G
INTRON31
Unknown significance
rs752046906
This variant is a VUS because it does not have enough information.
728889
chr6:70929843:->TCA
COL9A1
NM_078485:c.1853-3059_1853-3058insTGA
INTRON31
Benign
rs147934773
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
192
1322
0.1452
15
1006
0.0149
7
694
0.0101
121
1008
0.12
42
978
0.0429
377
5008
0.0752796
728890
chr6:70929843:->TCATCA
COL9A1
NM_078485:c.1853-3059_1853-3058insTGATGA
INTRON31
Benign
rs147934773
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
6
1322
0.0045
47
1006
0.0467
14
694
0.0202
7
1008
0.0069
61
978
0.0624
135
5008
0.0269569
728891
chr6:70929843:TCA>-
COL9A1
NM_078485:c.1853-3059_1853-3055delTGA
INTRON31
Benign
rs372560958
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
306
1322
0.2315
18
1006
0.0179
18
694
0.0259
14
1008
0.0139
10
978
0.0102
366
5008
0.0730831
728892
chr6:70929863:A>G
COL9A1
NM_078485:c.1853-3079T>C
INTRON31
Unknown significance
rs771360944
This variant is a VUS because it does not have enough information.
728893
chr6:70929910:->G
COL9A1
NM_078485:c.1853-3126_1853-3125insC
INTRON31
Unknown significance
rs398049030
This variant is a VUS because it does not have enough information.
728894
chr6:70929911:->T
COL9A1
NM_078485:c.1853-3127_1853-3126insA
INTRON31
Benign
rs59262394
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
456
1322
0.3449
295
1006
0.2932
322
694
0.464
441
1008
0.4375
257
978
0.2628
1771
5008
0.353634
728895
chr6:70929911:G>T
COL9A1
NM_078485:c.1853-3127C>A
INTRON31
Unknown significance
rs34892469
This variant is a VUS because it does not have enough information.
728896
chr6:70929911:GG>TGC
COL9A1
Unknown significance
rs386702484
This variant is a VUS because it does not have enough information.
728897
chr6:70929912:G>C
COL9A1
NM_078485:c.1853-3128C>G
INTRON31
Benign
rs58885304
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
399
1322
0.3018
236
1006
0.2346
249
694
0.3588
333
1008
0.3304
216
978
0.2209
1433
5008
0.286142
728898
chr6:70929913:->C
COL9A1
NM_078485:c.1853-3129_1853-3128insG
INTRON31
Unknown significance
rs200802448
This variant is a VUS because it does not have enough information.
728899
chr6:70929913:->TGC
COL9A1
NM_078485:c.1853-3129_1853-3128insGCA
INTRON31
Unknown significance
rs398049030
This variant is a VUS because it does not have enough information.
728900
chr6:70929916:A>G
COL9A1
NM_078485:c.1853-3132T>C
INTRON31
Unknown significance
rs534763131
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
0
694
0
0
1008
0
1
978
0.001
1
5008
0.000199681
728901
chr6:70929933:G>A
COL9A1
NM_078485:c.1853-3149C>T
INTRON31
Unknown significance
rs139228201
This variant is a VUS because it does not have enough information.
5
1322
0.0038
0
1006
0
1
694
0.0014
0
1008
0
0
978
0
6
5008
0.00119808
728902
chr6:70929946:T>G
COL9A1
NM_078485:c.1853-3162A>C
INTRON31
Unknown significance
rs777118692
This variant is a VUS because it does not have enough information.
728903
chr6:70929949:T>C
COL9A1
NM_078485:c.1853-3165A>G
INTRON31
Unknown significance
rs143255369
This variant is a VUS because it does not have enough information.
5
1322
0.0038
0
1006
0
0
694
0
0
1008
0
0
978
0
5
5008
0.000998403
728904
chr6:70930021:A>G
COL9A1
NM_078485:c.1853-3237T>C
INTRON31
Benign
rs190549423
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
9
1322
0.0068
0
1006
0
1
694
0.0014
0
1008
0
0
978
0
10
5008
0.00199681
728905
chr6:70930073:G>T
COL9A1
NM_078485:c.1853-3289C>A
INTRON31
Benign
rs1200567
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
301
1322
0.2277
47
1006
0.0467
27
694
0.0389
6
1008
0.006
60
978
0.0613
441
5008
0.0880591
728906
chr6:70930077:->G
COL9A1
NM_078485:c.1853-3293_1853-3292insC
INTRON31
Benign
rs150139945
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
294
1322
0.2224
0
1006
0
13
694
0.0187
0
1008
0
0
978
0
307
5008
0.0613019
728907
chr6:70930079:A>G
COL9A1
NM_078485:c.1853-3295T>C
INTRON31
Benign
rs28694097
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
381
1322
0.2882
48
1006
0.0477
31
694
0.0447
6
1008
0.006
60
978
0.0613
526
5008
0.105032
728908
chr6:70930088:G>T
COL9A1
NM_078485:c.1853-3304C>A
INTRON31
Unknown significance
rs539628320
This variant is a VUS because it does not have enough information.
5
1322
0.0038
0
1006
0
0
694
0
0
1008
0
0
978
0
5
5008
0.000998403
728909
chr6:70930093:->GTGT
COL9A1
NM_078485:c.1853-3309_1853-3308insACAC
INTRON31
Unknown significance
rs58525634
This variant is a VUS because it does not have enough information.
728910
chr6:70930093:GT>-
COL9A1
NM_078485:c.1853-3309_1853-3306delAC
INTRON31
Unknown significance
rs796970877
This variant is a VUS because it does not have enough information.
728911
chr6:70930093:GTGT>-
COL9A1
NM_078485:c.1853-3309_1853-3304delACAC
INTRON31
Unknown significance
rs71749691
This variant is a VUS because it does not have enough information.
728912
chr6:70930093:GTGTGT>-
COL9A1
NM_078485:c.1853-3309_1853-3302delACACAC
INTRON31
Unknown significance
rs72155096
This variant is a VUS because it does not have enough information.
728913
chr6:70930093:GTGTGTGT>-
COL9A1
NM_078485:c.1853-3309_1853-3300delACACACAC
INTRON31
Unknown significance
rs796404376
This variant is a VUS because it does not have enough information.
728914
chr6:70930094:->GT
COL9A1
NM_078485:c.1853-3310_1853-3309insAC
INTRON31
Unknown significance
rs71925903
This variant is a VUS because it does not have enough information.
728915
chr6:70930116:T>G
COL9A1
NM_078485:c.1853-3332A>C
INTRON31
Unknown significance
rs372974173
This variant is a VUS because it does not have enough information.
728916
chr6:70930117:GTG>-
COL9A1
NM_078485:c.1853-3333_1853-3329delCAC
INTRON31
Unknown significance
rs779178275
This variant is a VUS because it does not have enough information.
728917
chr6:70930117:GTGTGG>-
COL9A1
NM_078485:c.1853-3333_1853-3326delCCACAC
INTRON31
Unknown significance
rs763362636
This variant is a VUS because it does not have enough information.
728918
chr6:70930167:C>G
COL9A1
NM_078485:c.1853-3383G>C
INTRON31
Benign
rs539975140
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
0
1322
0
0
1006
0
0
694
0
0
1008
0
16
978
0.0164
16
5008
0.00319489
728919
chr6:70930233:T>C
COL9A1
NM_078485:c.1853-3449A>G
INTRON31
Unknown significance
rs371642043
This variant is a VUS because it does not have enough information.
728920
chr6:70930242:G>A
COL9A1
NM_078485:c.1853-3458C>T
INTRON31
Unknown significance
rs775544490
This variant is a VUS because it does not have enough information.
728921
chr6:70930257:AGAAATACCAG>-
COL9A1
NM_078485:c.1853-3473_1853-3461delCTGGTATTTCT
INTRON31
Unknown significance
rs529376743
This variant is a VUS because it does not have enough information.
5
1322
0.0038
0
1006
0
0
694
0
0
1008
0
0
978
0
5
5008
0.000998403
728922
chr6:70930269:G>A
COL9A1
NM_078485:c.1853-3485C>T
INTRON31
Unknown significance
rs74946925
This variant is a VUS because it does not have enough information.
728923
chr6:70930270:A>G
COL9A1
NM_078485:c.1853-3486T>C
INTRON31
Unknown significance
rs190019541
This variant is a VUS because it does not have enough information.
0
1322
0
2
1006
0.002
0
694
0
0
1008
0
0
978
0
2
5008
0.000399361
728925
chr6:70930288:C>G
COL9A1
NM_078485:c.1853-3504G>C
INTRON31
Unknown significance
rs562990686
This variant is a VUS because it does not have enough information.
728924
chr6:70930288:C>T
COL9A1
NM_078485:c.1853-3504G>A
INTRON31
Unknown significance
rs562990686
This variant is a VUS because it does not have enough information.
1
1322
0.0008
0
1006
0
0
694
0
0
1008
0
0
978
0
1
5008
0.000199681
728926
chr6:70930289:AT>-
COL9A1
NM_078485:c.1853-3505_1853-3502delAT
INTRON31
Benign
rs147184570
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
301
1322
0.2277
47
1006
0.0467
27
694
0.0389
7
1008
0.0069
61
978
0.0624
443
5008
0.0884585
728927
chr6:70930327:G>T
COL9A1
NM_078485:c.1853-3543C>A
INTRON31
Unknown significance
rs561641003
This variant is a VUS because it does not have enough information.
1
1322
0.0008
0
1006
0
0
694
0
0
1008
0
0
978
0
1
5008
0.000199681
728928
chr6:70930330:T>C
COL9A1
NM_078485:c.1853-3546A>G
INTRON31
Unknown significance
rs575132672
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
0
694
0
1
1008
0.001
0
978
0
1
5008
0.000199681
728929
chr6:70930407:A>C
COL9A1
NM_078485:c.1853-3623T>G
INTRON31
Unknown significance
rs763228947
This variant is a VUS because it does not have enough information.
728930
chr6:70930421:C>T
COL9A1
NM_078485:c.1853-3637G>A
INTRON31
Benign
rs16868775
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
80
1322
0.0605
252
1006
0.2505
293
694
0.4222
437
1008
0.4335
196
978
0.2004
1258
5008
0.251198
728931
chr6:70930429:C>T
COL9A1
NM_078485:c.1853-3645G>A
INTRON31
Benign
rs369314981
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
0
1322
0
0
1006
0
0
694
0
0
1008
0
10
978
0.0102
10
5008
0.00199681
728932
chr6:70930541:C>T
COL9A1
NM_078485:c.1853-3757G>A
INTRON31
Unknown significance
rs532692113
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
0
694
0
0
1008
0
1
978
0.001
1
5008
0.000199681
728933
chr6:70930595:T>G
COL9A1
NM_078485:c.1853-3811A>C
INTRON31
Unknown significance
rs546106909
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
0
694
0
2
1008
0.002
0
978
0
2
5008
0.000399361
728934
chr6:70930600:T>C
COL9A1
NM_078485:c.1853-3816A>G
INTRON31
Benign
rs540654
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
302
1322
0.2284
48
1006
0.0477
27
694
0.0389
7
1008
0.0069
61
978
0.0624
445
5008
0.0888578
728935
chr6:70930641:A>G
COL9A1
NM_078485:c.1853-3857T>C
INTRON31
Unknown significance
rs528670189
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
0
694
0
1
1008
0.001
0
978
0
1
5008
0.000199681
728936
chr6:70930649:A>T
COL9A1
NM_078485:c.1853-3865T>A
INTRON31
Unknown significance
rs546896150
This variant is a VUS because it does not have enough information.
728937
chr6:70930669:T>C
COL9A1
NM_078485:c.1853-3885A>G
INTRON31
Unknown significance
rs181043242
This variant is a VUS because it does not have enough information.
1
1322
0.0008
1
1006
0.001
0
694
0
0
1008
0
0
978
0
2
5008
0.000399361
728938
chr6:70930673:T>C
COL9A1
NM_078485:c.1853-3889A>G
INTRON31
Unknown significance
rs568506077
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
0
694
0
1
1008
0.001
0
978
0
1
5008
0.000199681
728939
chr6:70930697:ATTATGTA>-
COL9A1
NM_078485:c.1853-3913_1853-3904delTACATAAT
INTRON31
Unknown significance
rs532657922
This variant is a VUS because it does not have enough information.
728940
chr6:70930720:C>T
COL9A1
NM_078485:c.1853-3936G>A
INTRON31
Unknown significance
rs530924223
This variant is a VUS because it does not have enough information.
3
1322
0.0023
0
1006
0
0
694
0
0
1008
0
0
978
0
3
5008
0.000599042
728941
chr6:70930761:C>T
COL9A1
NM_078485:c.1853-3977G>A
INTRON31
Unknown significance
rs754695971
This variant is a VUS because it does not have enough information.
728942
chr6:70930801:->CA
COL9A1
NM_078485:c.1853-4017_1853-4016insTG
INTRON31
Unknown significance
rs758619700
This variant is a VUS because it does not have enough information.
728943
chr6:70930801:G>-
COL9A1
NM_078485:c.1853-4017delC
INTRON31
Unknown significance
rs766176027
This variant is a VUS because it does not have enough information.
728944
chr6:70930802:T>-
COL9A1
NM_078485:c.1853-4018delA
INTRON31
Benign
rs58207213
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
310
1322
0.2345
52
1006
0.0517
33
694
0.0476
16
1008
0.0159
70
978
0.0716
481
5008
0.0960463
728945
chr6:70930811:T>A
COL9A1
NM_078485:c.1853-4027A>T
INTRON31
Benign
rs185563256
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
11
1322
0.0083
20
1006
0.0199
6
694
0.0086
2
1008
0.002
2
978
0.002
41
5008
0.0081869
728946
chr6:70930888:G>A
COL9A1
NM_078485:c.1853-4104C>T
INTRON31
Unknown significance
rs747818184
This variant is a VUS because it does not have enough information.
728947
chr6:70930892:G>A
COL9A1
NM_078485:c.1853-4108C>T
INTRON31
Benign
rs9446211
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
79
1322
0.0598
1
1006
0.001
4
694
0.0058
0
1008
0
0
978
0
84
5008
0.0167732
728948
chr6:70930894:A>C
COL9A1
NM_078485:c.1853-4110T>G
INTRON31
Benign
rs7739562
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
82
1322
0.062
253
1006
0.2515
292
694
0.4207
437
1008
0.4335
200
978
0.2045
1264
5008
0.252396
728949
chr6:70930897:A>T
COL9A1
NM_078485:c.1853-4113T>A
INTRON31
Unknown significance
rs189582297
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
0
694
0
1
1008
0.001
0
978
0
1
5008
0.000199681
728950
chr6:70930907:C>A
COL9A1
NM_078485:c.1853-4123G>T
INTRON31
Unknown significance
rs569305235
This variant is a VUS because it does not have enough information.
728951
chr6:70930935:G>A
COL9A1
NM_078485:c.1853-4151C>T
INTRON31
Benign
rs79979095
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
98
1322
0.0741
0
1006
0
1
694
0.0014
0
1008
0
3
978
0.0031
102
5008
0.0203674
728952
chr6:70930995:G>C
COL9A1
NM_078485:c.1853-4211C>G
INTRON31
Unknown significance
rs182150578
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
0
694
0
1
1008
0.001
0
978
0
1
5008
0.000199681
728953
chr6:70930997:T>C
COL9A1
NM_078485:c.1853-4213A>G
INTRON31
Unknown significance
rs555438680
This variant is a VUS because it does not have enough information.
2
1322
0.0015
0
1006
0
0
694
0
0
1008
0
0
978
0
2
5008
0.000399361
728954
chr6:70931017:G>T
COL9A1
NM_078485:c.1853-4233C>A
INTRON31
Unknown significance
rs556589955
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
0
694
0
0
1008
0
2
978
0.002
2
5008
0.000399361
728955
chr6:70931045:G>A
COL9A1
NM_078485:c.1853-4261C>T
INTRON31
Benign
rs9455007
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
79
1322
0.0598
1
1006
0.001
4
694
0.0058
0
1008
0
0
978
0
84
5008
0.0167732
728956
chr6:70931054:A>G
COL9A1
NM_078485:c.1853-4270T>C
INTRON31
Unknown significance
rs557439487
This variant is a VUS because it does not have enough information.
1
1322
0.0008
0
1006
0
0
694
0
0
1008
0
0
978
0
1
5008
0.000199681
728957
chr6:70931056:A>-
COL9A1
NM_078485:c.1853-4272delT
INTRON31
Unknown significance
rs747678301
This variant is a VUS because it does not have enough information.
728958
chr6:70931090:G>A
COL9A1
NM_078485:c.1853-4306C>T
INTRON31
Unknown significance
rs577231648
This variant is a VUS because it does not have enough information.
5
1322
0.0038
0
1006
0
0
694
0
0
1008
0
0
978
0
5
5008
0.000998403
728959
chr6:70931091:C>G
COL9A1
NM_078485:c.1853-4307G>C
INTRON31
Unknown significance
rs186077774
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
0
694
0
1
1008
0.001
0
978
0
1
5008
0.000199681
728960
chr6:70931111:A>G
COL9A1
NM_078485:c.1853-4327T>C
INTRON31
Benign
rs1200566
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
381
1322
0.2882
48
1006
0.0477
31
694
0.0447
7
1008
0.0069
61
978
0.0624
528
5008
0.105431
728961
chr6:70931120:T>C
COL9A1
NM_078485:c.1853-4336A>G
INTRON31
Unknown significance
rs528659085
This variant is a VUS because it does not have enough information.
0
1322
0
1
1006
0.001
0
694
0
0
1008
0
1
978
0.001
2
5008
0.000399361
728962
chr6:70931151:G>T
COL9A1
NM_078485:c.1853-4367C>A
INTRON31
Unknown significance
rs624606
This variant is a VUS because it does not have enough information.
728963
chr6:70931196:C>T
COL9A1
NM_078485:c.1853-4412G>A
INTRON31
Unknown significance
rs144838255
This variant is a VUS because it does not have enough information.
4
1322
0.003
0
1006
0
0
694
0
0
1008
0
0
978
0
4
5008
0.000798722
728964
chr6:70931205:A>C
COL9A1
NM_078485:c.1853-4421T>G
INTRON31
Unknown significance
rs770088197
This variant is a VUS because it does not have enough information.
728965
chr6:70931224:T>C
COL9A1
NM_078485:c.1852+4411A>G
INTRON31
Unknown significance
rs562194696
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
0
694
0
0
1008
0
1
978
0.001
1
5008
0.000199681
728966
chr6:70931241:->A
COL9A1
NM_078485:c.1852+4394_1852+4395insT
INTRON31
Unknown significance
rs773232941
This variant is a VUS because it does not have enough information.
728967
chr6:70931325:C>A
COL9A1
NM_078485:c.1852+4310G>T
INTRON31
Unknown significance
rs530937279
This variant is a VUS because it does not have enough information.
1
1322
0.0008
0
1006
0
0
694
0
0
1008
0
0
978
0
1
5008
0.000199681
728968
chr6:70931330:T>C
COL9A1
NM_078485:c.1852+4305A>G
INTRON31
Unknown significance
rs775875005
This variant is a VUS because it does not have enough information.
728969
chr6:70931341:G>C
COL9A1
NM_078485:c.1852+4294C>G
INTRON31
Unknown significance
rs746733921
This variant is a VUS because it does not have enough information.
728970
chr6:70931369:CA>-
COL9A1
NM_078485:c.1852+4266_1852+4269delTG
INTRON31
Unknown significance
rs757985829
This variant is a VUS because it does not have enough information.
728971
chr6:70931426:T>C
COL9A1
NM_078485:c.1852+4209A>G
INTRON31
Benign
rs7744579
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
154
1322
0.1165
254
1006
0.2525
297
694
0.428
438
1008
0.4345
200
978
0.2045
1343
5008
0.268171
728972
chr6:70931430:T>C
COL9A1
NM_078485:c.1852+4205A>G
INTRON31
Unknown significance
rs148154183
This variant is a VUS because it does not have enough information.
0
1322
0
1
1006
0.001
0
694
0
0
1008
0
0
978
0
1
5008
0.000199681
728973
chr6:70931436:A>T
COL9A1
NM_078485:c.1852+4199T>A
INTRON31
Unknown significance
rs533375129
This variant is a VUS because it does not have enough information.
1
1322
0.0008
0
1006
0
0
694
0
0
1008
0
0
978
0
1
5008
0.000199681
728974
chr6:70931496:C>T
COL9A1
NM_078485:c.1852+4139G>A
INTRON31
Unknown significance
rs377628094
This variant is a VUS because it does not have enough information.
1
1322
0.0008
0
1006
0
0
694
0
0
1008
0
0
978
0
1
5008
0.000199681
728975
chr6:70931506:G>C
COL9A1
NM_078485:c.1852+4129C>G
INTRON31
Unknown significance
rs576408901
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
0
694
0
0
1008
0
1
978
0.001
1
5008
0.000199681
728976
chr6:70931512:A>G
COL9A1
NM_078485:c.1852+4123T>C
INTRON31
Benign
rs6902075
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
13
1322
0.0098
1
1006
0.001
0
694
0
0
1008
0
0
978
0
14
5008
0.00279553
728977
chr6:70931520:G>C
COL9A1
NM_078485:c.1852+4115C>G
INTRON31
Unknown significance
rs555309020
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
1
694
0.0014
0
1008
0
0
978
0
1
5008
0.000199681
728978
chr6:70931553:C>T
COL9A1
NM_078485:c.1852+4082G>A
INTRON31
Unknown significance
rs569053944
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
1
694
0.0014
0
1008
0
0
978
0
1
5008
0.000199681
728979
chr6:70931554:C>T
COL9A1
NM_078485:c.1852+4081G>A
INTRON31
Unknown significance
rs537508042
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
0
694
0
1
1008
0.001
0
978
0
1
5008
0.000199681
728980
chr6:70931555:G>C
COL9A1
NM_078485:c.1852+4080C>G
INTRON31
Unknown significance
rs557841659
This variant is a VUS because it does not have enough information.
0
1322
0
1
1006
0.001
0
694
0
0
1008
0
0
978
0
1
5008
0.000199681
728981
chr6:70931575:T>C
COL9A1
NM_078485:c.1852+4060A>G
INTRON31
Unknown significance
rs150709445
This variant is a VUS because it does not have enough information.
0
1322
0
2
1006
0.002
0
694
0
0
1008
0
2
978
0.002
4
5008
0.000798722
728982
chr6:70931584:G>A
COL9A1
NM_078485:c.1852+4051C>T
INTRON31
Unknown significance
rs761973528
This variant is a VUS because it does not have enough information.
728983
chr6:70931600:G>A
COL9A1
NM_078485:c.1852+4035C>T
INTRON31
Unknown significance
rs551388053
This variant is a VUS because it does not have enough information.
728984
chr6:70931614:T>G
COL9A1
NM_078485:c.1852+4021A>C
INTRON31
Unknown significance
rs539888219
This variant is a VUS because it does not have enough information.
0
1322
0
1
1006
0.001
0
694
0
0
1008
0
0
978
0
1
5008
0.000199681
728985
chr6:70931634:A>C
COL9A1
NM_078485:c.1852+4001T>G
INTRON31
Unknown significance
rs553239978
This variant is a VUS because it does not have enough information.
1
1322
0.0008
0
1006
0
0
694
0
0
1008
0
0
978
0
1
5008
0.000199681
728986
chr6:70931639:C>T
COL9A1
NM_078485:c.1852+3996G>A
INTRON31
Unknown significance
rs139114777
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
0
694
0
0
1008
0
0
978
0
0
5008
0
728987
chr6:70931670:C>T
COL9A1
NM_078485:c.1852+3965G>A
INTRON31
Unknown significance
rs753747874
This variant is a VUS because it does not have enough information.
728988
chr6:70931711:C>G
COL9A1
NM_078485:c.1852+3924G>C
INTRON31
Unknown significance
rs192288014
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
0
694
0
1
1008
0.001
0
978
0
1
5008
0.000199681
728989
chr6:70931733:T>G
COL9A1
NM_078485:c.1852+3902A>C
INTRON31
Benign
rs116364152
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
45
1322
0.034
0
1006
0
3
694
0.0043
0
1008
0
1
978
0.001
49
5008
0.00978435
728990
chr6:70931735:G>A
COL9A1
NM_078485:c.1852+3900C>T
INTRON31
Unknown significance
rs371356492
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
1
694
0.0014
0
1008
0
0
978
0
1
5008
0.000199681
728991
chr6:70931735:G>T
COL9A1
NM_078485:c.1852+3900C>A
INTRON31
Unknown significance
rs371356492
This variant is a VUS because it does not have enough information.
728992
chr6:70931749:C>T
COL9A1
NM_078485:c.1852+3886G>A
INTRON31
Unknown significance
rs544339355
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
0
694
0
1
1008
0.001
0
978
0
1
5008
0.000199681
728993
chr6:70931773:G>A
COL9A1
NM_078485:c.1852+3862C>T
INTRON31
Unknown significance
rs752422848
This variant is a VUS because it does not have enough information.
728994
chr6:70931777:A>G
COL9A1
NM_078485:c.1852+3858T>C
INTRON31
Unknown significance
rs564576470
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
0
694
0
0
1008
0
1
978
0.001
1
5008
0.000199681
728995
chr6:70931780:T>C
COL9A1
NM_078485:c.1852+3855A>G
INTRON31
Unknown significance
rs764312897
This variant is a VUS because it does not have enough information.
728996
chr6:70931783:A>G
COL9A1
NM_078485:c.1852+3852T>C
INTRON31
Unknown significance
rs373962684
This variant is a VUS because it does not have enough information.
728997
chr6:70931798:A>T
COL9A1
NM_078485:c.1852+3837T>A
INTRON31
Unknown significance
rs184072885
This variant is a VUS because it does not have enough information.
1
1322
0.0008
0
1006
0
0
694
0
0
1008
0
0
978
0
1
5008
0.000199681
728998
chr6:70931802:C>T
COL9A1
NM_078485:c.1852+3833G>A
INTRON31
Unknown significance
rs547059114
This variant is a VUS because it does not have enough information.
1
1322
0.0008
0
1006
0
0
694
0
0
1008
0
0
978
0
1
5008
0.000199681
728999
chr6:70931809:G>A
COL9A1
NM_078485:c.1852+3826C>T
INTRON31
Unknown significance
rs560462303
This variant is a VUS because it does not have enough information.
2
1322
0.0015
0
1006
0
0
694
0
0
1008
0
0
978
0
2
5008
0.000399361
729000
chr6:70931829:T>C
COL9A1
NM_078485:c.1852+3806A>G
INTRON31
Unknown significance
rs188507339
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
0
694
0
1
1008
0.001
0
978
0
1
5008
0.000199681
729001
chr6:70931855:T>C
COL9A1
NM_078485:c.1852+3780A>G
INTRON31
Unknown significance
rs533877889
This variant is a VUS because it does not have enough information.
729002
chr6:70931865:A>G
COL9A1
NM_078485:c.1852+3770T>C
INTRON31
Unknown significance
rs549272338
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
1
694
0.0014
0
1008
0
0
978
0
1
5008
0.000199681
729003
chr6:70931872:T>C
COL9A1
NM_078485:c.1852+3763A>G
INTRON31
Unknown significance
rs758113310
This variant is a VUS because it does not have enough information.
729004
chr6:70931875:->A
COL9A1
NM_078485:c.1852+3760_1852+3761insT
INTRON31
Unknown significance
rs774347435
This variant is a VUS because it does not have enough information.
729005
chr6:70931902:T>C
COL9A1
NM_078485:c.1852+3733A>G
INTRON31
Unknown significance
rs777389066
This variant is a VUS because it does not have enough information.
729006
chr6:70931930:T>A
COL9A1
NM_078485:c.1852+3705A>T
INTRON31
Unknown significance
rs761912725
This variant is a VUS because it does not have enough information.
729007
chr6:70931940:A>G
COL9A1
NM_078485:c.1852+3695T>C
INTRON31
Unknown significance
rs751117689
This variant is a VUS because it does not have enough information.
729008
chr6:70931948:G>C
COL9A1
NM_078485:c.1852+3687C>G
INTRON31
Unknown significance
rs568916790
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
0
694
0
0
1008
0
1
978
0.001
1
5008
0.000199681
729009
chr6:70931970:A>G
COL9A1
NM_078485:c.1852+3665T>C
INTRON31
Unknown significance
rs538046057
This variant is a VUS because it does not have enough information.
0
1322
0
1
1006
0.001
0
694
0
0
1008
0
0
978
0
1
5008
0.000199681
729010
chr6:70931998:A>T
COL9A1
NM_078485:c.1852+3637T>A
INTRON31
Unknown significance
rs553874932
This variant is a VUS because it does not have enough information.
729011
chr6:70932059:A>G
COL9A1
NM_078485:c.1852+3576T>C
INTRON31
Unknown significance
rs192240046
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
0
694
0
1
1008
0.001
1
978
0.001
2
5008
0.000399361
729012
chr6:70932137:T>C
COL9A1
NM_078485:c.1852+3498A>G
INTRON31
Unknown significance
rs571048331
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
0
694
0
1
1008
0.001
0
978
0
1
5008
0.000199681
729013
chr6:70932153:T>C
COL9A1
NM_078485:c.1852+3482A>G
INTRON31
Unknown significance
rs533529004
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
0
694
0
0
1008
0
1
978
0.001
1
5008
0.000199681
729014
chr6:70932158:C>T
COL9A1
NM_078485:c.1852+3477G>A
INTRON31
Unknown significance
rs756692530
This variant is a VUS because it does not have enough information.
729015
chr6:70932180:A>G
COL9A1
NM_078485:c.1852+3455T>C
INTRON31
Unknown significance
rs182542086
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
1
694
0.0014
0
1008
0
0
978
0
1
5008
0.000199681
729016
chr6:70932183:C>T
COL9A1
NM_078485:c.1852+3452G>A
INTRON31
Unknown significance
rs573323724
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
0
694
0
0
1008
0
1
978
0.001
1
5008
0.000199681
729017
chr6:70932236:C>T
COL9A1
NM_078485:c.1852+3399G>A
INTRON31
Unknown significance
rs377115112
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
0
694
0
2
1008
0.002
0
978
0
2
5008
0.000399361
729018
chr6:70932245:C>A
COL9A1
NM_078485:c.1852+3390G>T
INTRON31
Unknown significance
rs370521337
This variant is a VUS because it does not have enough information.
729019
chr6:70932272:T>C
COL9A1
NM_078485:c.1852+3363A>G
INTRON31
Unknown significance
rs556035919
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
0
694
0
1
1008
0.001
0
978
0
1
5008
0.000199681
729020
chr6:70932274:T>A
COL9A1
NM_078485:c.1852+3361A>T
INTRON31
Benign
rs542213342
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
0
1322
0
0
1006
0
0
694
0
0
1008
0
13
978
0.0133
13
5008
0.00259585
729021
chr6:70932279:C>G
COL9A1
NM_078485:c.1852+3356G>C
INTRON31
Benign
rs3806066
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
75
1322
0.0567
254
1006
0.2525
293
694
0.4222
438
1008
0.4345
194
978
0.1984
1254
5008
0.250399
729022
chr6:70932340:C>T
COL9A1
NM_078485:c.1852+3295G>A
INTRON31
Unknown significance
rs564564043
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
0
694
0
0
1008
0
1
978
0.001
1
5008
0.000199681
729023
chr6:70932357:C>G
COL9A1
NM_078485:c.1852+3278G>C
INTRON31
Unknown significance
rs578170329
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
0
694
0
0
1008
0
1
978
0.001
1
5008
0.000199681
729024
chr6:70932365:A>C
COL9A1
NM_078485:c.1852+3270T>G
INTRON31
Unknown significance
rs577315779
This variant is a VUS because it does not have enough information.
729025
chr6:70932378:G>A
COL9A1
NM_078485:c.1852+3257C>T
INTRON31
Benign
rs187094267
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
0
1322
0
1
1006
0.001
2
694
0.0029
0
1008
0
6
978
0.0061
9
5008
0.00179712
729026
chr6:70932393:A>G
COL9A1
NM_078485:c.1852+3242T>C
INTRON31
Unknown significance
rs769060551
This variant is a VUS because it does not have enough information.
729027
chr6:70932395:C>T
COL9A1
NM_078485:c.1852+3240G>A
INTRON31
Unknown significance
rs560481212
This variant is a VUS because it does not have enough information.
1
1322
0.0008
0
1006
0
1
694
0.0014
0
1008
0
1
978
0.001
3
5008
0.000599042
729028
chr6:70932396:G>A
COL9A1
NM_078485:c.1852+3239C>T
INTRON31
Benign
rs191861799
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
0
1322
0
0
1006
0
10
694
0.0144
0
1008
0
1
978
0.001
11
5008
0.00219649
729029
chr6:70932423:C>-
COL9A1
NM_078485:c.1852+3212delG
INTRON31
Benign
rs140881955
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
25
1322
0.0189
0
1006
0
2
694
0.0029
0
1008
0
0
978
0
27
5008
0.00539137
729030
chr6:70932442:C>T
COL9A1
NM_078485:c.1852+3193G>A
INTRON31
Unknown significance
rs75885355
This variant is a VUS because it does not have enough information.
729031
chr6:70932443:->T
COL9A1
NM_078485:c.1852+3192_1852+3193insA
INTRON31
Benign
rs543872078
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
105
1322
0.0794
265
1006
0.2634
295
694
0.4251
425
1008
0.4216
209
978
0.2137
1299
5008
0.259385
729032
chr6:70932443:T>C
COL9A1
NM_078485:c.1852+3192A>G
INTRON31
Unknown significance
rs75543099
This variant is a VUS because it does not have enough information.
729033
chr6:70932446:->TC
COL9A1
NM_078485:c.1852+3189_1852+3190insGA
INTRON31
Benign
rs200198798
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
79
1322
0.0598
1
1006
0.001
4
694
0.0058
0
1008
0
0
978
0
84
5008
0.0167732
729034
chr6:70932447:->C
COL9A1
NM_078485:c.1852+3188_1852+3189insG
INTRON31
Unknown significance
rs58197230
This variant is a VUS because it does not have enough information.
729035
chr6:70932449:T>A
COL9A1
NM_078485:c.1852+3186A>T
INTRON31
Benign
rs184458645
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
9
1322
0.0068
0
1006
0
1
694
0.0014
0
1008
0
0
978
0
10
5008
0.00199681
729036
chr6:70932453:T>A
COL9A1
NM_078485:c.1852+3182A>T
INTRON31
Unknown significance
rs79093438
This variant is a VUS because it does not have enough information.
729037
chr6:70932454:T>A
COL9A1
NM_078485:c.1852+3181A>T
INTRON31
Unknown significance
rs80042938
This variant is a VUS because it does not have enough information.
729038
chr6:70932480:C>A
COL9A1
NM_078485:c.1852+3155G>T
INTRON31
Unknown significance
rs562846743
This variant is a VUS because it does not have enough information.
2
1322
0.0015
0
1006
0
0
694
0
0
1008
0
0
978
0
2
5008
0.000399361
729039
chr6:70932492:A>G
COL9A1
NM_078485:c.1852+3143T>C
INTRON31
Unknown significance
rs531395411
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
0
694
0
2
1008
0.002
0
978
0
2
5008
0.000399361
729040
chr6:70932513:T>A
COL9A1
NM_078485:c.1852+3122A>T
INTRON31
Unknown significance
rs774695937
This variant is a VUS because it does not have enough information.
729041
chr6:70932535:A>C
COL9A1
NM_078485:c.1852+3100T>G
INTRON31
Benign
rs1210977
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
1313
1322
0.9932
748
1006
0.7435
605
694
0.8718
947
1008
0.9395
767
978
0.7843
4380
5008
0.874601
729042
chr6:70932568:C>T
COL9A1
NM_078485:c.1852+3067G>A
INTRON31
Unknown significance
rs556523947
This variant is a VUS because it does not have enough information.
729043
chr6:70932569:G>A
COL9A1
NM_078485:c.1852+3066C>T
INTRON31
Benign
rs144029464
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
0
1322
0
9
1006
0.0089
2
694
0.0029
0
1008
0
1
978
0.001
12
5008
0.00239617
729044
chr6:70932604:A>C
COL9A1
NM_078485:c.1852+3031T>G
INTRON31
Benign
rs9360416
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
285
1322
0.2156
396
1006
0.3936
222
694
0.3199
132
1008
0.131
396
978
0.4049
1431
5008
0.285743
729045
chr6:70932636:T>C
COL9A1
NM_078485:c.1852+2999A>G
INTRON31
Unknown significance
rs765216160
This variant is a VUS because it does not have enough information.
729046
chr6:70932645:G>C
COL9A1
NM_078485:c.1852+2990C>G
INTRON31
Unknown significance
rs547106137
This variant is a VUS because it does not have enough information.
1
1322
0.0008
0
1006
0
0
694
0
0
1008
0
0
978
0
1
5008
0.000199681
729047
chr6:70932703:G>A
COL9A1
NM_078485:c.1852+2932C>T
INTRON31
Benign
rs189332350
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
0
1322
0
6
1006
0.006
0
694
0
0
1008
0
0
978
0
6
5008
0.00119808
729048
chr6:70932738:T>C
COL9A1
NM_078485:c.1852+2897A>G
INTRON31
Unknown significance
rs111850492
This variant is a VUS because it does not have enough information.
729049
chr6:70932751:A>C
COL9A1
NM_078485:c.1852+2884T>G
INTRON31
Unknown significance
rs374594455
This variant is a VUS because it does not have enough information.
729050
chr6:70932756:T>G
COL9A1
NM_078485:c.1852+2879A>C
INTRON31
Unknown significance
rs145979152
This variant is a VUS because it does not have enough information.
0
1322
0
2
1006
0.002
0
694
0
0
1008
0
0
978
0
2
5008
0.000399361
729051
chr6:70932782:T>C
COL9A1
NM_078485:c.1852+2853A>G
INTRON31
Unknown significance
rs763774819
This variant is a VUS because it does not have enough information.
729052
chr6:70932792:T>C
COL9A1
NM_078485:c.1852+2843A>G
INTRON31
Unknown significance
rs555784475
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
0
694
0
2
1008
0.002
0
978
0
2
5008
0.000399361
729053
chr6:70932802:G>A
COL9A1
NM_078485:c.1852+2833C>T
INTRON31
Unknown significance
rs193212365
This variant is a VUS because it does not have enough information.
1
1322
0.0008
0
1006
0
0
694
0
0
1008
0
0
978
0
1
5008
0.000199681
729054
chr6:70932818:C>A
COL9A1
NM_078485:c.1852+2817G>T
INTRON31
Benign
rs185562481
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
0
1322
0
0
1006
0
6
694
0.0086
0
1008
0
0
978
0
6
5008
0.00119808
729055
chr6:70932819:G>A
COL9A1
NM_078485:c.1852+2816C>T
INTRON31
Unknown significance
rs573469725
This variant is a VUS because it does not have enough information.
729056
chr6:70932858:A>G
COL9A1
NM_078485:c.1852+2777T>C
INTRON31
Unknown significance
rs540777846
This variant is a VUS because it does not have enough information.
729057
chr6:70932861:G>A
COL9A1
NM_078485:c.1852+2774C>T
INTRON31
Benign
rs1200565
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
295
1322
0.2231
47
1006
0.0467
27
694
0.0389
7
1008
0.0069
61
978
0.0624
437
5008
0.0872604
729058
chr6:70932861:G>C
COL9A1
NM_078485:c.1852+2774C>G
INTRON31
Unknown significance
rs1200565
This variant is a VUS because it does not have enough information.
729059
chr6:70932884:G>A
COL9A1
NM_078485:c.1852+2751C>T
INTRON31
Unknown significance
rs578226128
This variant is a VUS because it does not have enough information.
4
1322
0.003
0
1006
0
0
694
0
0
1008
0
0
978
0
4
5008
0.000798722
729060
chr6:70932900:A>G
COL9A1
NM_078485:c.1852+2735T>C
INTRON31
Unknown significance
rs372302835
This variant is a VUS because it does not have enough information.
729061
chr6:70932911:A>G
COL9A1
NM_078485:c.1852+2724T>C
INTRON31
Benign
rs1200564
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
292
1322
0.2209
47
1006
0.0467
27
694
0.0389
7
1008
0.0069
61
978
0.0624
434
5008
0.0866613
729062
chr6:70932974:->A
COL9A1
NM_078485:c.1852+2661_1852+2662insT
INTRON31
Unknown significance
rs551119800
This variant is a VUS because it does not have enough information.
0
1322
0
1
1006
0.001
1
694
0.0014
0
1008
0
1
978
0.001
3
5008
0.000599042
729063
chr6:70932991:C>T
COL9A1
NM_078485:c.1852+2644G>A
INTRON31
Unknown significance
rs139912515
This variant is a VUS because it does not have enough information.
1
1322
0.0008
0
1006
0
0
694
0
0
1008
0
0
978
0
1
5008
0.000199681
729064
chr6:70932992:G>A
COL9A1
NM_078485:c.1852+2643C>T
INTRON31
Unknown significance
rs573946501
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
0
694
0
1
1008
0.001
0
978
0
1
5008
0.000199681
729066
chr6:70933038:T>C
COL9A1
NM_078485:c.1852+2597A>G
INTRON31
Unknown significance
rs543047023
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
0
694
0
0
1008
0
1
978
0.001
1
5008
0.000199681
729065
chr6:70933038:TTTC>-
COL9A1
NM_078485:c.1852+2597_1852+2602delGAAA
INTRON31
Unknown significance
rs796606487
This variant is a VUS because it does not have enough information.
729067
chr6:70933063:A>G
COL9A1
NM_078485:c.1852+2572T>C
INTRON31
Unknown significance
rs562623698
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
0
694
0
0
1008
0
1
978
0.001
1
5008
0.000199681
729068
chr6:70933090:T>A
COL9A1
NM_078485:c.1852+2545A>T
INTRON31
Benign
rs78737155
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
1
1322
0.0008
47
1006
0.0467
14
694
0.0202
7
1008
0.0069
61
978
0.0624
130
5008
0.0259585
729069
chr6:70933127:G>C
COL9A1
NM_078485:c.1852+2508C>G
INTRON31
Unknown significance
rs375023220
This variant is a VUS because it does not have enough information.
729070
chr6:70933169:A>T
COL9A1
NM_078485:c.1852+2466T>A
INTRON31
Benign
rs4707705
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
159
1322
0.1203
255
1006
0.2535
296
694
0.4265
437
1008
0.4335
194
978
0.1984
1341
5008
0.267772
729071
chr6:70933172:C>T
COL9A1
NM_078485:c.1852+2463G>A
INTRON31
Benign
rs564704853
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
0
1322
0
0
1006
0
0
694
0
9
1008
0.0089
0
978
0
9
5008
0.00179712
729072
chr6:70933173:G>A
COL9A1
NM_078485:c.1852+2462C>T
INTRON31
Benign
rs527492585
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
9
1322
0.0068
0
1006
0
1
694
0.0014
0
1008
0
0
978
0
10
5008
0.00199681
729073
chr6:70933175:G>A
COL9A1
NM_078485:c.1852+2460C>T
INTRON31
Benign
rs4707706
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
159
1322
0.1203
255
1006
0.2535
296
694
0.4265
437
1008
0.4335
194
978
0.1984
1341
5008
0.267772
729074
chr6:70933185:T>C
COL9A1
NM_078485:c.1852+2450A>G
INTRON31
Unknown significance
rs567401798
This variant is a VUS because it does not have enough information.
2
1322
0.0015
0
1006
0
0
694
0
0
1008
0
0
978
0
2
5008
0.000399361
729075
chr6:70933186:->G
COL9A1
NM_078485:c.1852+2449_1852+2450insC
INTRON31
Unknown significance
rs780667775
This variant is a VUS because it does not have enough information.
729076
chr6:70933196:T>C
COL9A1
NM_078485:c.1852+2439A>G
INTRON31
Unknown significance
rs534657618
This variant is a VUS because it does not have enough information.
2
1322
0.0015
0
1006
0
0
694
0
0
1008
0
0
978
0
2
5008
0.000399361
729077
chr6:70933251:A>G
COL9A1
NM_078485:c.1852+2384T>C
INTRON31
Unknown significance
rs188834862
This variant is a VUS because it does not have enough information.
3
1322
0.0023
0
1006
0
0
694
0
0
1008
0
0
978
0
3
5008
0.000599042
729078
chr6:70933286:G>A
COL9A1
NM_078485:c.1852+2349C>T
INTRON31
Unknown significance
rs779369523
This variant is a VUS because it does not have enough information.
729079
chr6:70933290:A>C
COL9A1
NM_078485:c.1852+2345T>G
INTRON31
Unknown significance
rs768822172
This variant is a VUS because it does not have enough information.
729080
chr6:70933297:C>T
COL9A1
NM_078485:c.1852+2338G>A
INTRON31
Unknown significance
rs569431578
This variant is a VUS because it does not have enough information.
0
1322
0
1
1006
0.001
0
694
0
0
1008
0
0
978
0
1
5008
0.000199681
729081
chr6:70933298:G>A
COL9A1
NM_078485:c.1852+2337C>T
INTRON31
Benign
rs9455008
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
34
1322
0.0257
1
1006
0.001
1
694
0.0014
0
1008
0
0
978
0
36
5008
0.0071885
729082
chr6:70933302:T>A
COL9A1
NM_078485:c.1852+2333A>T
INTRON31
Unknown significance
rs555741372
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
0
694
0
0
1008
0
1
978
0.001
1
5008
0.000199681
729083
chr6:70933306:C>G
COL9A1
NM_078485:c.1852+2329G>C
INTRON31
Unknown significance
rs374772995
This variant is a VUS because it does not have enough information.
729084
chr6:70933315:G>A
COL9A1
NM_078485:c.1852+2320C>T
INTRON31
Unknown significance
rs748328288
This variant is a VUS because it does not have enough information.
729085
chr6:70933332:C>G
COL9A1
NM_078485:c.1852+2303G>C
INTRON31
Unknown significance
rs112256737
This variant is a VUS because it does not have enough information.
729086
chr6:70933350:G>A
COL9A1
NM_078485:c.1852+2285C>T
INTRON31
Unknown significance
rs772267468
This variant is a VUS because it does not have enough information.
729087
chr6:70933361:C>T
COL9A1
NM_078485:c.1852+2274G>A
INTRON31
Unknown significance
rs368905442
This variant is a VUS because it does not have enough information.
729088
chr6:70933370:C>G
COL9A1
NM_078485:c.1852+2265G>C
INTRON31
Unknown significance
rs571820513
This variant is a VUS because it does not have enough information.
0
1322
0
1
1006
0.001
0
694
0
0
1008
0
0
978
0
1
5008
0.000199681