552671
chr3:45430090:G>T
LARS2
NM_015340:c.-170G>T
FIVE_PRIME_EXON
Benign
rs558984490
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
16
1322
0.0121
0
1006
0
1
694
0.0014
0
1008
0
0
978
0
17
5008
0.00339457
552672
chr3:45430095:T>C
LARS2
NM_015340:c.-165T>C
FIVE_PRIME_EXON
Unknown significance
rs375274687
This variant is a VUS because it does not have enough information.
552673
chr3:45430104:G>T
LARS2
NM_015340:c.-156G>T
FIVE_PRIME_EXON
Unknown significance
rs577271414
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
552675
chr3:45430114:G>A
LARS2
NM_015340:c.-146G>A
FIVE_PRIME_EXON
Unknown significance
rs73830406
This variant is a VUS because it does not have enough information.
552674
chr3:45430114:G>T
LARS2
NM_015340:c.-146G>T
FIVE_PRIME_EXON
Benign
rs73830406
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
49
1322
0.0371
1
1006
0.001
4
694
0.0058
0
1008
0
0
978
0
54
5008
0.0107827
552676
chr3:45430118:G>A
LARS2
NM_015340:c.-142G>A
FIVE_PRIME_EXON
Unknown significance
rs187335191
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
552677
chr3:45430151:G>A
LARS2
NM_015340:c.-109G>A
FIVE_PRIME_EXON
Benign
rs28413188
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
123
1322
0.093
290
1006
0.2883
98
694
0.1412
114
1008
0.1131
182
978
0.1861
807
5008
0.161142
552678
chr3:45430178:C>T
LARS2
NM_015340:c.-88+6C>T
FIVE_PRIME_INTRON
Unknown significance
rs767039300
This variant is a VUS because it does not have enough information.
552679
chr3:45430202:G>C
LARS2
NM_015340:c.-88+30G>C
FIVE_PRIME_INTRON
Unknown significance
rs752131388
This variant is a VUS because it does not have enough information.
552680
chr3:45430224:C>A
LARS2
NM_015340:c.-88+52C>A
FIVE_PRIME_INTRON
Unknown significance
rs577863209
This variant is a VUS because it does not have enough information.
552681
chr3:45430224:C>G
LARS2
NM_015340:c.-88+52C>G
FIVE_PRIME_INTRON
Unknown significance
rs577863209
This variant is a VUS because it does not have enough information.
552682
chr3:45430237:G>T
LARS2
NM_015340:c.-88+65G>T
FIVE_PRIME_INTRON
Unknown significance
rs369735137
This variant is a VUS because it does not have enough information.
552683
chr3:45430245:C>G
LARS2
NM_015340:c.-88+73C>G
FIVE_PRIME_INTRON
Benign
rs9860885
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
243
1322
0.1838
186
1006
0.1849
98
694
0.1412
7
1008
0.0069
137
978
0.1401
671
5008
0.133986
552684
chr3:45430260:C>G
LARS2
NM_015340:c.-88+88C>G
FIVE_PRIME_INTRON
Unknown significance
rs191270808
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
552685
chr3:45430271:G>A
LARS2
NM_015340:c.-88+99G>A
FIVE_PRIME_INTRON
Unknown significance
rs375761741
This variant is a VUS because it does not have enough information.
552686
chr3:45430279:C>T
LARS2
NM_015340:c.-88+107C>T
FIVE_PRIME_INTRON
Unknown significance
rs753374341
This variant is a VUS because it does not have enough information.
552687
chr3:45430322:A>C
LARS2
NM_015340:c.-88+150A>C
FIVE_PRIME_INTRON
Unknown significance
rs575842786
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
552688
chr3:45430342:C>A
LARS2
NM_015340:c.-88+170C>A
FIVE_PRIME_INTRON
Benign
rs147089747
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
1
1322
0.0008
12
1006
0.0119
4
694
0.0058
0
1008
0
7
978
0.0072
24
5008
0.00479233
552689
chr3:45430363:C>A
LARS2
NM_015340:c.-88+191C>A
FIVE_PRIME_INTRON
Unknown significance
rs373260201
This variant is a VUS because it does not have enough information.
552690
chr3:45430371:T>C
LARS2
NM_015340:c.-88+199T>C
FIVE_PRIME_INTRON
Unknown significance
rs142764310
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
552691
chr3:45430379:G>C
LARS2
NM_015340:c.-88+207G>C
FIVE_PRIME_INTRON
Unknown significance
rs778256614
This variant is a VUS because it does not have enough information.
552692
chr3:45430409:C>T
LARS2
NM_015340:c.-88+237C>T
FIVE_PRIME_INTRON
Unknown significance
rs768679316
This variant is a VUS because it does not have enough information.
552693
chr3:45430415:T>G
LARS2
NM_015340:c.-88+243T>G
FIVE_PRIME_INTRON
Unknown significance
rs745433365
This variant is a VUS because it does not have enough information.
552694
chr3:45430431:C>G
LARS2
NM_015340:c.-88+259C>G
FIVE_PRIME_INTRON
Benign
rs531934510
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
7
1008
0.0069
0
978
0
7
5008
0.00139776
552695
chr3:45430435:T>C
LARS2
NM_015340:c.-88+263T>C
FIVE_PRIME_INTRON
Unknown significance
rs547106248
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
552696
chr3:45430462:G>T
LARS2
NM_015340:c.-88+290G>T
FIVE_PRIME_INTRON
Unknown significance
rs376246201
This variant is a VUS because it does not have enough information.
552697
chr3:45430475:G>A
LARS2
NM_015340:c.-88+303G>A
FIVE_PRIME_INTRON
Benign
rs147976827
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
1
1322
0.0008
12
1006
0.0119
4
694
0.0058
0
1008
0
7
978
0.0072
24
5008
0.00479233
552698
chr3:45430483:G>A
LARS2
NM_015340:c.-88+311G>A
FIVE_PRIME_INTRON
Unknown significance
rs529928668
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
2
694
0.0029
0
1008
0
0
978
0
2
5008
0.000399361
552699
chr3:45430489:G>A
LARS2
NM_015340:c.-88+317G>A
FIVE_PRIME_INTRON
Unknown significance
rs548080414
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
552701
chr3:45430517:G>A
LARS2
NM_015340:c.-88+345G>A
FIVE_PRIME_INTRON
Unknown significance
rs199535431
This variant is a VUS because it does not have enough information.
552700
chr3:45430517:G>C
LARS2
NM_015340:c.-88+345G>C
FIVE_PRIME_INTRON
Unknown significance
rs199535431
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
552702
chr3:45430555:C>T
LARS2
NM_015340:c.-88+383C>T
FIVE_PRIME_INTRON
Unknown significance
rs536957807
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
552703
chr3:45430562:A>G
LARS2
NM_015340:c.-88+390A>G
FIVE_PRIME_INTRON
Unknown significance
rs746955963
This variant is a VUS because it does not have enough information.
552704
chr3:45430585:G>A
LARS2
NM_015340:c.-88+413G>A
FIVE_PRIME_INTRON
Unknown significance
rs768384297
This variant is a VUS because it does not have enough information.
552705
chr3:45430596:C>T
LARS2
NM_015340:c.-88+424C>T
FIVE_PRIME_INTRON
Unknown significance
rs776551269
This variant is a VUS because it does not have enough information.
552706
chr3:45430623:A>G
LARS2
NM_015340:c.-88+451A>G
FIVE_PRIME_INTRON
Unknown significance
rs552457193
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
552707
chr3:45430626:->T
LARS2
NM_015340:c.-88+454_-88+455insT
FIVE_PRIME_INTRON
Unknown significance
rs551967501
This variant is a VUS because it does not have enough information.
1
1322
0.0008
1
1006
0.001
0
694
0
1
1008
0.001
0
978
0
3
5008
0.000599042
552708
chr3:45430647:T>G
LARS2
NM_015340:c.-88+475T>G
FIVE_PRIME_INTRON
Unknown significance
rs748032807
This variant is a VUS because it does not have enough information.
552709
chr3:45430659:A>G
LARS2
NM_015340:c.-88+487A>G
FIVE_PRIME_INTRON
Unknown significance
rs772177428
This variant is a VUS because it does not have enough information.
552710
chr3:45430716:C>T
LARS2
NM_015340:c.-88+544C>T
FIVE_PRIME_INTRON
Unknown significance
rs193114605
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
0
694
0
4
1008
0.004
0
978
0
4
5008
0.000798722
552711
chr3:45430717:C>T
LARS2
NM_015340:c.-88+545C>T
FIVE_PRIME_INTRON
Unknown significance
rs76716023
This variant is a VUS because it does not have enough information.
6
1322
0.0045
1
1006
0.001
0
694
0
0
1008
0
0
978
0
7
5008
0.00139776
552712
chr3:45430730:->C
LARS2
NM_015340:c.-88+558_-88+559insC
FIVE_PRIME_INTRON
Unknown significance
rs34331179
This variant is a VUS because it does not have enough information.
552713
chr3:45430764:C>T
LARS2
NM_015340:c.-88+592C>T
FIVE_PRIME_INTRON
Unknown significance
rs553536442
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
552714
chr3:45430766:C>T
LARS2
NM_015340:c.-88+594C>T
FIVE_PRIME_INTRON
Unknown significance
rs761932423
This variant is a VUS because it does not have enough information.
552715
chr3:45430784:A>G
LARS2
NM_015340:c.-88+612A>G
FIVE_PRIME_INTRON
Unknown significance
rs770090843
This variant is a VUS because it does not have enough information.
552716
chr3:45430819:A>G
LARS2
NM_015340:c.-88+647A>G
FIVE_PRIME_INTRON
Unknown significance
rs552952652
This variant is a VUS because it does not have enough information.
552717
chr3:45430819:A>T
LARS2
NM_015340:c.-88+647A>T
FIVE_PRIME_INTRON
Unknown significance
rs552952652
This variant is a VUS because it does not have enough information.
552718
chr3:45430830:G>A
LARS2
NM_015340:c.-88+658G>A
FIVE_PRIME_INTRON
Unknown significance
rs540373687
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
552719
chr3:45430833:G>A
LARS2
NM_015340:c.-88+661G>A
FIVE_PRIME_INTRON
Unknown significance
rs370247964
This variant is a VUS because it does not have enough information.
552720
chr3:45430835:G>A
LARS2
NM_015340:c.-88+663G>A
FIVE_PRIME_INTRON
Benign
rs113258506
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
552721
chr3:45430878:C>T
LARS2
NM_015340:c.-88+706C>T
FIVE_PRIME_INTRON
Benign
rs9865493
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
144
1322
0.1089
0
1006
0
4
694
0.0058
0
1008
0
0
978
0
148
5008
0.0295527
552722
chr3:45430916:A>G
LARS2
NM_015340:c.-88+744A>G
FIVE_PRIME_INTRON
Unknown significance
rs147343640
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
4
978
0.0041
5
5008
0.000998403
552723
chr3:45430928:G>T
LARS2
NM_015340:c.-88+756G>T
FIVE_PRIME_INTRON
Unknown significance
rs752043511
This variant is a VUS because it does not have enough information.
552724
chr3:45430999:C>T
LARS2
NM_015340:c.-88+827C>T
FIVE_PRIME_INTRON
Unknown significance
rs377114824
This variant is a VUS because it does not have enough information.
552725
chr3:45431012:->AGG
LARS2
NM_015340:c.-88+840_-88+841insAGG
FIVE_PRIME_INTRON
Unknown significance
rs570437554
This variant is a VUS because it does not have enough information.
552726
chr3:45431014:C>G
LARS2
NM_015340:c.-88+842C>G
FIVE_PRIME_INTRON
Unknown significance
rs370818645
This variant is a VUS because it does not have enough information.
552727
chr3:45431061:A>G
LARS2
NM_015340:c.-88+889A>G
FIVE_PRIME_INTRON
Unknown significance
rs546092177
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
552728
chr3:45431062:G>T
LARS2
NM_015340:c.-88+890G>T
FIVE_PRIME_INTRON
Unknown significance
rs760133468
This variant is a VUS because it does not have enough information.
552729
chr3:45431065:C>T
LARS2
NM_015340:c.-88+893C>T
FIVE_PRIME_INTRON
Benign
rs73068222
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
0
1322
0
41
1006
0.0408
16
694
0.0231
0
1008
0
9
978
0.0092
66
5008
0.0131789
552730
chr3:45431094:T>A
LARS2
NM_015340:c.-88+922T>A
FIVE_PRIME_INTRON
Unknown significance
rs576465238
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
552731
chr3:45431132:G>C
LARS2
NM_015340:c.-88+960G>C
FIVE_PRIME_INTRON
Unknown significance
rs540603526
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
552732
chr3:45431145:G>T
LARS2
NM_015340:c.-88+973G>T
FIVE_PRIME_INTRON
Benign
rs115527080
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
1
1322
0.0008
18
1006
0.0179
12
694
0.0173
0
1008
0
1
978
0.001
32
5008
0.00638978
552733
chr3:45431151:A>C
LARS2
NM_015340:c.-88+979A>C
FIVE_PRIME_INTRON
Unknown significance
rs568565964
This variant is a VUS because it does not have enough information.
552734
chr3:45431151:A>G
LARS2
NM_015340:c.-88+979A>G
FIVE_PRIME_INTRON
Unknown significance
rs568565964
This variant is a VUS because it does not have enough information.
552735
chr3:45431153:TCT>-
LARS2
NM_015340:c.-88+981_-88+983delTCT
FIVE_PRIME_INTRON
Unknown significance
rs111324141
This variant is a VUS because it does not have enough information.
552736
chr3:45431158:T>C
LARS2
NM_015340:c.-88+986T>C
FIVE_PRIME_INTRON
Unknown significance
rs529744891
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
552737
chr3:45431166:G>C
LARS2
NM_015340:c.-88+994G>C
FIVE_PRIME_INTRON
Benign
rs185834174
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
10
1322
0.0076
0
1006
0
0
694
0
0
1008
0
0
978
0
10
5008
0.00199681
552738
chr3:45431206:C>G
LARS2
NM_015340:c.-88+1034C>G
FIVE_PRIME_INTRON
Unknown significance
rs563342771
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
552739
chr3:45431261:C>G
LARS2
NM_015340:c.-88+1089C>G
FIVE_PRIME_INTRON
Unknown significance
rs188863189
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
2
694
0.0029
0
1008
0
0
978
0
2
5008
0.000399361
552740
chr3:45431289:G>C
LARS2
NM_015340:c.-88+1117G>C
FIVE_PRIME_INTRON
Unknown significance
rs192292773
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
552741
chr3:45431324:A>G
LARS2
NM_015340:c.-88+1152A>G
FIVE_PRIME_INTRON
Unknown significance
rs570741066
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
552742
chr3:45431327:C>T
LARS2
NM_015340:c.-88+1155C>T
FIVE_PRIME_INTRON
Benign
rs114302553
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
39
1322
0.0295
0
1006
0
0
694
0
0
1008
0
0
978
0
39
5008
0.00778754
552743
chr3:45431421:T>C
LARS2
NM_015340:c.-88+1249T>C
FIVE_PRIME_INTRON
Unknown significance
rs547012113
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
552744
chr3:45431481:G>A
LARS2
NM_015340:c.-88+1309G>A
FIVE_PRIME_INTRON
Unknown significance
rs183960583
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
552745
chr3:45431485:T>G
LARS2
NM_015340:c.-88+1313T>G
FIVE_PRIME_INTRON
Unknown significance
rs375536288
This variant is a VUS because it does not have enough information.
552746
chr3:45431494:G>A
LARS2
NM_015340:c.-88+1322G>A
FIVE_PRIME_INTRON
Unknown significance
rs535586496
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
552747
chr3:45431551:C>T
LARS2
NM_015340:c.-88+1379C>T
FIVE_PRIME_INTRON
Benign
rs188575376
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
1
694
0.0014
0
1008
0
1
978
0.001
8
5008
0.00159744
552748
chr3:45431554:AC>-
LARS2
NM_015340:c.-88+1382_-88+1383delAC
FIVE_PRIME_INTRON
Unknown significance
rs548529803
This variant is a VUS because it does not have enough information.
1
1322
0.0008
2
1006
0.002
0
694
0
0
1008
0
1
978
0.001
4
5008
0.000798722
552749
chr3:45431581:C>T
LARS2
NM_015340:c.-88+1409C>T
FIVE_PRIME_INTRON
Unknown significance
rs757839713
This variant is a VUS because it does not have enough information.
552750
chr3:45431585:A>C
LARS2
NM_015340:c.-88+1413A>C
FIVE_PRIME_INTRON
Unknown significance
rs569372466
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
552751
chr3:45431592:GGT>-
LARS2
NM_015340:c.-88+1420_-88+1422delGGT
FIVE_PRIME_INTRON
Benign
rs552818948
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
15
1322
0.0113
0
1006
0
1
694
0.0014
0
1008
0
0
978
0
16
5008
0.00319489
552753
chr3:45431640:T>C
LARS2
NM_015340:c.-87-1435T>C
FIVE_PRIME_INTRON
Unknown significance
rs368564023
This variant is a VUS because it does not have enough information.
552752
chr3:45431640:TTTCT>-
LARS2
NM_015340:c.-87-1435_-87-1431delTTTCT
FIVE_PRIME_INTRON
Unknown significance
rs143722017
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
1
978
0.001
3
5008
0.000599042
552754
chr3:45431657:A>G
LARS2
NM_015340:c.-87-1418A>G
FIVE_PRIME_INTRON
Unknown significance
rs137891799
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
552755
chr3:45431674:T>G
LARS2
NM_015340:c.-87-1401T>G
FIVE_PRIME_INTRON
Benign
rs62244085
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
4
1322
0.003
99
1006
0.0984
125
694
0.1801
256
1008
0.254
60
978
0.0613
544
5008
0.108626
552756
chr3:45431706:T>C
LARS2
NM_015340:c.-87-1369T>C
FIVE_PRIME_INTRON
Unknown significance
rs765826022
This variant is a VUS because it does not have enough information.
552757
chr3:45431725:A>G
LARS2
NM_015340:c.-87-1350A>G
FIVE_PRIME_INTRON
Unknown significance
rs376024655
This variant is a VUS because it does not have enough information.
552758
chr3:45431873:C>T
LARS2
NM_015340:c.-87-1202C>T
FIVE_PRIME_INTRON
Unknown significance
rs573198544
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
552759
chr3:45431980:A>G
LARS2
NM_015340:c.-87-1095A>G
FIVE_PRIME_INTRON
Benign
rs540667863
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
1
1322
0.0008
0
1006
0
0
694
0
0
1008
0
5
978
0.0051
6
5008
0.00119808
552760
chr3:45431983:T>G
LARS2
NM_015340:c.-87-1092T>G
FIVE_PRIME_INTRON
Unknown significance
rs552704959
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
552761
chr3:45432017:G>C
LARS2
NM_015340:c.-87-1058G>C
FIVE_PRIME_INTRON
Unknown significance
rs533830950
This variant is a VUS because it does not have enough information.
552762
chr3:45432073:G>C
LARS2
NM_015340:c.-87-1002G>C
FIVE_PRIME_INTRON
Benign
rs180673990
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
552763
chr3:45432099:G>A
LARS2
NM_015340:c.-87-976G>A
FIVE_PRIME_INTRON
Unknown significance
rs541585266
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
552764
chr3:45432112:C>A
LARS2
NM_015340:c.-87-963C>A
FIVE_PRIME_INTRON
Unknown significance
rs563363878
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
552765
chr3:45432115:->T
LARS2
NM_015340:c.-87-960_-87-959insT
FIVE_PRIME_INTRON
Unknown significance
rs61446397
This variant is a VUS because it does not have enough information.
552766
chr3:45432127:->TTAT
LARS2
NM_015340:c.-87-948_-87-947insTTAT
FIVE_PRIME_INTRON
Unknown significance
rs752081850
This variant is a VUS because it does not have enough information.
552767
chr3:45432127:TTAT>-
LARS2
NM_015340:c.-87-948_-87-945delTTAT
FIVE_PRIME_INTRON
Unknown significance
rs373874105
This variant is a VUS because it does not have enough information.
552768
chr3:45432139:T>G
LARS2
NM_015340:c.-87-936T>G
FIVE_PRIME_INTRON
Unknown significance
rs530757392
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
552769
chr3:45432174:T>C
LARS2
NM_015340:c.-87-901T>C
FIVE_PRIME_INTRON
Benign
rs545995464
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
13
1322
0.0098
0
1006
0
1
694
0.0014
0
1008
0
0
978
0
14
5008
0.00279553
552770
chr3:45432233:C>T
LARS2
NM_015340:c.-87-842C>T
FIVE_PRIME_INTRON
Unknown significance
rs746939982
This variant is a VUS because it does not have enough information.
552771
chr3:45432259:C>G
LARS2
NM_015340:c.-87-816C>G
FIVE_PRIME_INTRON
Unknown significance
rs564417911
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
552772
chr3:45432327:G>A
LARS2
NM_015340:c.-87-748G>A
FIVE_PRIME_INTRON
Unknown significance
rs553791065
This variant is a VUS because it does not have enough information.
552773
chr3:45432343:A>T
LARS2
NM_015340:c.-87-732A>T
FIVE_PRIME_INTRON
Unknown significance
rs528382858
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
552774
chr3:45432379:G>A
LARS2
NM_015340:c.-87-696G>A
FIVE_PRIME_INTRON
Unknown significance
rs367835290
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
552775
chr3:45432383:C>T
LARS2
NM_015340:c.-87-692C>T
FIVE_PRIME_INTRON
Benign
rs854188
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
540
1322
0.4085
50
1006
0.0497
60
694
0.0865
125
1008
0.124
65
978
0.0665
840
5008
0.167732
552776
chr3:45432411:C>T
LARS2
NM_015340:c.-87-664C>T
FIVE_PRIME_INTRON
Unknown significance
rs529259405
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
552777
chr3:45432414:G>A
LARS2
NM_015340:c.-87-661G>A
FIVE_PRIME_INTRON
Unknown significance
rs550811784
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
552778
chr3:45432422:G>A
LARS2
NM_015340:c.-87-653G>A
FIVE_PRIME_INTRON
Unknown significance
rs569312929
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
552779
chr3:45432423:C>T
LARS2
NM_015340:c.-87-652C>T
FIVE_PRIME_INTRON
Benign
rs115353662
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
1
1322
0.0008
70
1006
0.0696
17
694
0.0245
0
1008
0
3
978
0.0031
91
5008
0.0181709
552780
chr3:45432443:T>C
LARS2
NM_015340:c.-87-632T>C
FIVE_PRIME_INTRON
Unknown significance
rs780815258
This variant is a VUS because it does not have enough information.
552781
chr3:45432476:C>A
LARS2
NM_015340:c.-87-599C>A
FIVE_PRIME_INTRON
Benign
rs72881341
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
88
1322
0.0666
0
1006
0
3
694
0.0043
0
1008
0
0
978
0
91
5008
0.0181709
552782
chr3:45432479:A>G
LARS2
NM_015340:c.-87-596A>G
FIVE_PRIME_INTRON
Benign
rs72881342
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
144
1322
0.1089
0
1006
0
4
694
0.0058
0
1008
0
0
978
0
148
5008
0.0295527
552783
chr3:45432490:A>G
LARS2
NM_015340:c.-87-585A>G
FIVE_PRIME_INTRON
Benign
rs144134097
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
24
1322
0.0182
0
1006
0
0
694
0
0
1008
0
0
978
0
24
5008
0.00479233
552784
chr3:45432504:G>A
LARS2
NM_015340:c.-87-571G>A
FIVE_PRIME_INTRON
Unknown significance
rs555999263
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
552785
chr3:45432532:C>T
LARS2
NM_015340:c.-87-543C>T
FIVE_PRIME_INTRON
Unknown significance
rs752994187
This variant is a VUS because it does not have enough information.
552786
chr3:45432533:G>A
LARS2
NM_015340:c.-87-542G>A
FIVE_PRIME_INTRON
Benign
rs148692937
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
12
1322
0.0091
0
1006
0
0
694
0
0
1008
0
0
978
0
12
5008
0.00239617
552787
chr3:45432554:A>C
LARS2
NM_015340:c.-87-521A>C
FIVE_PRIME_INTRON
Benign
rs854189
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
830
1322
0.6278
373
1006
0.3708
186
694
0.268
342
1008
0.3393
340
978
0.3476
2071
5008
0.413538
552788
chr3:45432696:G>A
LARS2
NM_015340:c.-87-379G>A
FIVE_PRIME_INTRON
Unknown significance
rs767217220
This variant is a VUS because it does not have enough information.
552789
chr3:45432697:T>C
LARS2
NM_015340:c.-87-378T>C
FIVE_PRIME_INTRON
Unknown significance
rs556804657
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
2
694
0.0029
0
1008
0
0
978
0
2
5008
0.000399361
552790
chr3:45432706:G>A
LARS2
NM_015340:c.-87-369G>A
FIVE_PRIME_INTRON
Benign
rs62244086
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
135
1322
0.1021
290
1006
0.2883
98
694
0.1412
114
1008
0.1131
181
978
0.1851
818
5008
0.163339
552791
chr3:45432709:G>A
LARS2
NM_015340:c.-87-366G>A
FIVE_PRIME_INTRON
Unknown significance
rs755641727
This variant is a VUS because it does not have enough information.
552792
chr3:45432760:G>A
LARS2
NM_015340:c.-87-315G>A
FIVE_PRIME_INTRON
Unknown significance
rs372043078
This variant is a VUS because it does not have enough information.
552793
chr3:45432769:A>G
LARS2
NM_015340:c.-87-306A>G
FIVE_PRIME_INTRON
Unknown significance
rs371672601
This variant is a VUS because it does not have enough information.
552794
chr3:45432805:G>A
LARS2
NM_015340:c.-87-270G>A
FIVE_PRIME_INTRON
Benign
rs142141083
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
17
1008
0.0169
1
978
0.001
18
5008
0.00359425
552795
chr3:45432814:A>G
LARS2
NM_015340:c.-87-261A>G
FIVE_PRIME_INTRON
Benign
rs111912927
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
168
1322
0.1271
0
1006
0
4
694
0.0058
0
1008
0
0
978
0
172
5008
0.034345
552796
chr3:45432821:C>T
LARS2
NM_015340:c.-87-254C>T
FIVE_PRIME_INTRON
Benign
rs573713411
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
25
978
0.0256
25
5008
0.00499201
552797
chr3:45432845:C>-
LARS2
NM_015340:c.-87-230delC
FIVE_PRIME_INTRON
Unknown significance
rs562063072
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
552798
chr3:45432860:C>G
LARS2
NM_015340:c.-87-215C>G
FIVE_PRIME_INTRON
Unknown significance
rs540177697
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
552799
chr3:45432904:G>A
LARS2
NM_015340:c.-87-171G>A
FIVE_PRIME_INTRON
Unknown significance
rs779679742
This variant is a VUS because it does not have enough information.
552800
chr3:45432918:A>C
LARS2
NM_015340:c.-87-157A>C
FIVE_PRIME_INTRON
Benign
rs561982863
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
7
1322
0.0053
0
1006
0
0
694
0
0
1008
0
0
978
0
7
5008
0.00139776
552801
chr3:45432928:G>T
LARS2
NM_015340:c.-87-147G>T
FIVE_PRIME_INTRON
Unknown significance
rs533663871
This variant is a VUS because it does not have enough information.
552802
chr3:45432933:C>T
LARS2
NM_015340:c.-87-142C>T
FIVE_PRIME_INTRON
Unknown significance
rs375242150
This variant is a VUS because it does not have enough information.
552803
chr3:45432934:G>A
LARS2
NM_015340:c.-87-141G>A
FIVE_PRIME_INTRON
Unknown significance
rs529299007
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
552804
chr3:45432954:C>T
LARS2
NM_015340:c.-87-121C>T
FIVE_PRIME_INTRON
Unknown significance
rs186031757
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
552805
chr3:45432976:->A
LARS2
NM_015340:c.-87-99_-87-98insA
FIVE_PRIME_INTRON
Unknown significance
rs537703578
This variant is a VUS because it does not have enough information.
552806
chr3:45432987:A>C
LARS2
NM_015340:c.-87-88A>C
FIVE_PRIME_INTRON
Unknown significance
rs574452203
This variant is a VUS because it does not have enough information.
552807
chr3:45432994:A>G
LARS2
NM_015340:c.-87-81A>G
FIVE_PRIME_INTRON
Unknown significance
rs190486665
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
552808
chr3:45433018:A>C
LARS2
NM_015340:c.-87-57A>C
FIVE_PRIME_INTRON
Unknown significance
rs79138815
This variant is a VUS because it does not have enough information.
552809
chr3:45433101:A>-
LARS2
NM_015340:c.-61delA
FIVE_PRIME_EXON
Benign
rs149976694
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
37
1322
0.028
0
1006
0
0
694
0
0
1008
0
0
978
0
37
5008
0.00738818
552810
chr3:45433110:A>G
LARS2
NM_015340:c.-52A>G
FIVE_PRIME_EXON
Unknown significance
rs182031628
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
552811
chr3:45433126:G>A
LARS2
NM_015340:c.-36G>A
FIVE_PRIME_EXON
Benign
rs75054661
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
75
1322
0.0567
32
1006
0.0318
25
694
0.036
103
1008
0.1022
94
978
0.0961
329
5008
0.0656949
552812
chr3:45433153:TTTT>-
LARS2
NM_015340:c.-22+13_-22+16delTTTT
FIVE_PRIME_INTRON
Unknown significance
rs773235116
This variant is a VUS because it does not have enough information.
552813
chr3:45433209:T>-
LARS2
NM_015340:c.-22+69delT
FIVE_PRIME_INTRON
Unknown significance
rs760495919
This variant is a VUS because it does not have enough information.
552814
chr3:45433245:C>T
LARS2
NM_015340:c.-22+105C>T
FIVE_PRIME_INTRON
Unknown significance
rs186524490
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
552815
chr3:45433267:C>G
LARS2
NM_015340:c.-22+127C>G
FIVE_PRIME_INTRON
Benign
rs78674974
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
50
1322
0.0378
45
1006
0.0447
27
694
0.0389
125
1008
0.124
66
978
0.0675
313
5008
0.0625
552816
chr3:45433300:T>G
LARS2
NM_015340:c.-22+160T>G
FIVE_PRIME_INTRON
Unknown significance
rs778974440
This variant is a VUS because it does not have enough information.
552817
chr3:45433305:A>C
LARS2
NM_015340:c.-22+165A>C
FIVE_PRIME_INTRON
Unknown significance
rs549449047
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
552818
chr3:45433328:A>G
LARS2
NM_015340:c.-22+188A>G
FIVE_PRIME_INTRON
Unknown significance
rs774630588
This variant is a VUS because it does not have enough information.
552819
chr3:45433365:G>A
LARS2
NM_015340:c.-22+225G>A
FIVE_PRIME_INTRON
Unknown significance
rs376420330
This variant is a VUS because it does not have enough information.
552820
chr3:45433376:G>A
LARS2
NM_015340:c.-22+236G>A
FIVE_PRIME_INTRON
Unknown significance
rs190620375
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
552821
chr3:45433425:A>G
LARS2
NM_015340:c.-22+285A>G
FIVE_PRIME_INTRON
Unknown significance
rs140057266
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
552822
chr3:45433450:C>T
LARS2
NM_015340:c.-22+310C>T
FIVE_PRIME_INTRON
Unknown significance
rs556905520
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
552823
chr3:45433476:C>G
LARS2
NM_015340:c.-22+336C>G
FIVE_PRIME_INTRON
Unknown significance
rs572557044
This variant is a VUS because it does not have enough information.
552824
chr3:45433525:C>T
LARS2
NM_015340:c.-22+385C>T
FIVE_PRIME_INTRON
Unknown significance
rs575268572
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
552825
chr3:45433526:G>A
LARS2
NM_015340:c.-22+386G>A
FIVE_PRIME_INTRON
Unknown significance
rs539540504
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
552826
chr3:45433546:A>G
LARS2
NM_015340:c.-22+406A>G
FIVE_PRIME_INTRON
Unknown significance
rs546480520
This variant is a VUS because it does not have enough information.
552827
chr3:45433571:A>C
LARS2
NM_015340:c.-22+431A>C
FIVE_PRIME_INTRON
Unknown significance
rs11921382
This variant is a VUS because it does not have enough information.
552828
chr3:45433631:A>-
LARS2
NM_015340:c.-22+491delA
FIVE_PRIME_INTRON
Unknown significance
rs753270482
This variant is a VUS because it does not have enough information.
552829
chr3:45433646:T>A
LARS2
NM_015340:c.-22+506T>A
FIVE_PRIME_INTRON
Unknown significance
rs535970733
This variant is a VUS because it does not have enough information.
552830
chr3:45433649:C>T
LARS2
NM_015340:c.-22+509C>T
FIVE_PRIME_INTRON
Unknown significance
rs143676850
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
552831
chr3:45433664:C>T
LARS2
NM_015340:c.-22+524C>T
FIVE_PRIME_INTRON
Unknown significance
rs183173672
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
552832
chr3:45433665:G>A
LARS2
NM_015340:c.-22+525G>A
FIVE_PRIME_INTRON
Benign
rs114618641
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
3
1322
0.0023
14
1006
0.0139
3
694
0.0043
0
1008
0
0
978
0
20
5008
0.00399361
552833
chr3:45433673:A>G
LARS2
NM_015340:c.-22+533A>G
FIVE_PRIME_INTRON
Unknown significance
rs561880404
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
552834
chr3:45433684:C>G
LARS2
NM_015340:c.-22+544C>G
FIVE_PRIME_INTRON
Unknown significance
rs185524821
This variant is a VUS because it does not have enough information.
552835
chr3:45433717:A>G
LARS2
NM_015340:c.-22+577A>G
FIVE_PRIME_INTRON
Unknown significance
rs761062940
This variant is a VUS because it does not have enough information.
552836
chr3:45433725:A>G
LARS2
NM_015340:c.-22+585A>G
FIVE_PRIME_INTRON
Unknown significance
rs369027022
This variant is a VUS because it does not have enough information.
552837
chr3:45433728:G>A
LARS2
NM_015340:c.-22+588G>A
FIVE_PRIME_INTRON
Unknown significance
rs369688293
This variant is a VUS because it does not have enough information.
552838
chr3:45433775:A>G
LARS2
NM_015340:c.-22+635A>G
FIVE_PRIME_INTRON
Unknown significance
rs573870807
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
552839
chr3:45433777:A>G
LARS2
NM_015340:c.-22+637A>G
FIVE_PRIME_INTRON
Unknown significance
rs191274086
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
552840
chr3:45433795:->T
LARS2
NM_015340:c.-22+655_-22+656insT
FIVE_PRIME_INTRON
Unknown significance
rs749403733
This variant is a VUS because it does not have enough information.
552841
chr3:45433832:C>T
LARS2
NM_015340:c.-22+692C>T
FIVE_PRIME_INTRON
Unknown significance
rs562548408
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
552842
chr3:45433833:G>A
LARS2
NM_015340:c.-22+693G>A
FIVE_PRIME_INTRON
Benign
rs140446003
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
26
1008
0.0258
1
978
0.001
27
5008
0.00539137
552843
chr3:45433856:C>T
LARS2
NM_015340:c.-22+716C>T
FIVE_PRIME_INTRON
Unknown significance
rs371713584
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
552844
chr3:45433857:G>A
LARS2
NM_015340:c.-22+717G>A
FIVE_PRIME_INTRON
Unknown significance
rs560200856
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
552845
chr3:45433888:G>A
LARS2
NM_015340:c.-22+748G>A
FIVE_PRIME_INTRON
Unknown significance
rs527911314
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
552846
chr3:45433924:T>A
LARS2
NM_015340:c.-22+784T>A
FIVE_PRIME_INTRON
Unknown significance
rs531711321
This variant is a VUS because it does not have enough information.
552847
chr3:45433931:T>G
LARS2
NM_015340:c.-22+791T>G
FIVE_PRIME_INTRON
Unknown significance
rs771868235
This variant is a VUS because it does not have enough information.
552848
chr3:45433946:C>A
LARS2
NM_015340:c.-22+806C>A
FIVE_PRIME_INTRON
Unknown significance
rs78954836
This variant is a VUS because it does not have enough information.
552849
chr3:45433948:A>G
LARS2
NM_015340:c.-22+808A>G
FIVE_PRIME_INTRON
Unknown significance
rs764371892
This variant is a VUS because it does not have enough information.
552850
chr3:45433962:T>-
LARS2
NM_015340:c.-22+822delT
FIVE_PRIME_INTRON
Unknown significance
rs771636912
This variant is a VUS because it does not have enough information.
552851
chr3:45433976:G>-
LARS2
NM_015340:c.-22+836delG
FIVE_PRIME_INTRON
Unknown significance
rs78074624
This variant is a VUS because it does not have enough information.
552852
chr3:45433979:G>A
LARS2
NM_015340:c.-22+839G>A
FIVE_PRIME_INTRON
Unknown significance
rs77165393
This variant is a VUS because it does not have enough information.
552853
chr3:45434003:T>C
LARS2
NM_015340:c.-22+863T>C
FIVE_PRIME_INTRON
Unknown significance
rs77450529
This variant is a VUS because it does not have enough information.
552854
chr3:45434007:G>A
LARS2
NM_015340:c.-22+867G>A
FIVE_PRIME_INTRON
Unknown significance
rs76878712
This variant is a VUS because it does not have enough information.
552855
chr3:45434041:C>T
LARS2
NM_015340:c.-22+901C>T
FIVE_PRIME_INTRON
Unknown significance
rs549548349
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
552856
chr3:45434055:G>A
LARS2
NM_015340:c.-22+915G>A
FIVE_PRIME_INTRON
Unknown significance
rs372950545
This variant is a VUS because it does not have enough information.
552857
chr3:45434066:C>T
LARS2
NM_015340:c.-22+926C>T
FIVE_PRIME_INTRON
Benign
rs74329574
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
39
1008
0.0387
0
978
0
39
5008
0.00778754
552858
chr3:45434078:C>T
LARS2
NM_015340:c.-22+938C>T
FIVE_PRIME_INTRON
Unknown significance
rs758107377
This variant is a VUS because it does not have enough information.
552859
chr3:45434082:T>C
LARS2
NM_015340:c.-22+942T>C
FIVE_PRIME_INTRON
Unknown significance
rs765874417
This variant is a VUS because it does not have enough information.
552860
chr3:45434091:A>G
LARS2
NM_015340:c.-22+951A>G
FIVE_PRIME_INTRON
Benign
rs543320834
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
9
978
0.0092
9
5008
0.00179712
552861
chr3:45434096:->T
LARS2
NM_015340:c.-22+956_-22+957insT
FIVE_PRIME_INTRON
Unknown significance
rs374588804
This variant is a VUS because it does not have enough information.
552862
chr3:45434112:T>C
LARS2
NM_015340:c.-22+972T>C
FIVE_PRIME_INTRON
Unknown significance
rs751105709
This variant is a VUS because it does not have enough information.
552863
chr3:45434126:T>A
LARS2
NM_015340:c.-22+986T>A
FIVE_PRIME_INTRON
Unknown significance
rs550448578
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
552864
chr3:45434139:A>G
LARS2
NM_015340:c.-22+999A>G
FIVE_PRIME_INTRON
Unknown significance
rs563010271
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
3
978
0.0031
4
5008
0.000798722
552865
chr3:45434169:A>G
LARS2
NM_015340:c.-22+1029A>G
FIVE_PRIME_INTRON
Unknown significance
rs539405182
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
552866
chr3:45434171:G>A
LARS2
NM_015340:c.-22+1031G>A
FIVE_PRIME_INTRON
Unknown significance
rs777924226
This variant is a VUS because it does not have enough information.
552867
chr3:45434175:A>G
LARS2
NM_015340:c.-22+1035A>G
FIVE_PRIME_INTRON
Unknown significance
rs747262647
This variant is a VUS because it does not have enough information.
552868
chr3:45434220:G>A
LARS2
NM_015340:c.-22+1080G>A
FIVE_PRIME_INTRON
Benign
rs557920576
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
7
1322
0.0053
0
1006
0
0
694
0
0
1008
0
0
978
0
7
5008
0.00139776
552869
chr3:45434256:A>G
LARS2
NM_015340:c.-22+1116A>G
FIVE_PRIME_INTRON
Unknown significance
rs781132524
This variant is a VUS because it does not have enough information.
552870
chr3:45434338:A>G
LARS2
NM_015340:c.-22+1198A>G
FIVE_PRIME_INTRON
Unknown significance
rs748064782
This variant is a VUS because it does not have enough information.
552871
chr3:45434351:A>G
LARS2
NM_015340:c.-22+1211A>G
FIVE_PRIME_INTRON
Unknown significance
rs370618024
This variant is a VUS because it does not have enough information.
552872
chr3:45434363:C>T
LARS2
NM_015340:c.-22+1223C>T
FIVE_PRIME_INTRON
Unknown significance
rs182672377
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
552873
chr3:45434403:G>T
LARS2
NM_015340:c.-22+1263G>T
FIVE_PRIME_INTRON
Benign
rs854190
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
1322
1322
1
1006
1006
1
694
694
1
1008
1008
1
978
978
1
5008
5008
1
552874
chr3:45434411:T>C
LARS2
NM_015340:c.-22+1271T>C
FIVE_PRIME_INTRON
Unknown significance
rs777723105
This variant is a VUS because it does not have enough information.
552875
chr3:45434478:G>A
LARS2
NM_015340:c.-22+1338G>A
FIVE_PRIME_INTRON
Unknown significance
rs555548361
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
552876
chr3:45434485:T>G
LARS2
NM_015340:c.-22+1345T>G
FIVE_PRIME_INTRON
Benign
rs56183927
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
56
1322
0.0424
1
1006
0.001
4
694
0.0058
0
1008
0
0
978
0
61
5008
0.0121805
552877
chr3:45434496:T>C
LARS2
NM_015340:c.-22+1356T>C
FIVE_PRIME_INTRON
Unknown significance
rs771346308
This variant is a VUS because it does not have enough information.
552878
chr3:45434513:C>T
LARS2
NM_015340:c.-22+1373C>T
FIVE_PRIME_INTRON
Unknown significance
rs544519351
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
552879
chr3:45434519:C>T
LARS2
NM_015340:c.-22+1379C>T
FIVE_PRIME_INTRON
Unknown significance
rs373217605
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
552880
chr3:45434561:A>G
LARS2
NM_015340:c.-21-1364A>G
FIVE_PRIME_INTRON
Unknown significance
rs377667882
This variant is a VUS because it does not have enough information.
552881
chr3:45434591:A>G
LARS2
NM_015340:c.-21-1334A>G
FIVE_PRIME_INTRON
Unknown significance
rs577653086
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
552882
chr3:45434601:A>C
LARS2
NM_015340:c.-21-1324A>C
FIVE_PRIME_INTRON
Unknown significance
rs771187317
This variant is a VUS because it does not have enough information.
552883
chr3:45434618:C>T
LARS2
NM_015340:c.-21-1307C>T
FIVE_PRIME_INTRON
Unknown significance
rs776673207
This variant is a VUS because it does not have enough information.
552884
chr3:45434656:G>A
LARS2
NM_015340:c.-21-1269G>A
FIVE_PRIME_INTRON
Unknown significance
rs544982212
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
552885
chr3:45434674:C>T
LARS2
NM_015340:c.-21-1251C>T
FIVE_PRIME_INTRON
Unknown significance
rs187557003
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
552886
chr3:45434679:C>T
LARS2
NM_015340:c.-21-1246C>T
FIVE_PRIME_INTRON
Benign
rs149219761
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
63
1322
0.0477
0
1006
0
1
694
0.0014
0
1008
0
1
978
0.001
65
5008
0.0129792
552887
chr3:45434683:A>G
LARS2
NM_015340:c.-21-1242A>G
FIVE_PRIME_INTRON
Unknown significance
rs146710677
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
552888
chr3:45434688:AT>-
LARS2
NM_015340:c.-21-1237_-21-1236delAT
FIVE_PRIME_INTRON
Unknown significance
rs561976818
This variant is a VUS because it does not have enough information.
552889
chr3:45434690:G>A
LARS2
NM_015340:c.-21-1235G>A
FIVE_PRIME_INTRON
Unknown significance
rs139260158
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
552890
chr3:45434709:C>T
LARS2
NM_015340:c.-21-1216C>T
FIVE_PRIME_INTRON
Benign
rs854191
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
1304
1322
0.9864
814
1006
0.8091
466
694
0.6715
423
1008
0.4196
668
978
0.683
3675
5008
0.733826
552891
chr3:45434740:T>C
LARS2
NM_015340:c.-21-1185T>C
FIVE_PRIME_INTRON
Unknown significance
rs761102406
This variant is a VUS because it does not have enough information.
552892
chr3:45434755:A>G
LARS2
NM_015340:c.-21-1170A>G
FIVE_PRIME_INTRON
Unknown significance
rs550510748
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
552894
chr3:45434758:TA>-
LARS2
NM_015340:c.-21-1167_-21-1166delTA
FIVE_PRIME_INTRON
Unknown significance
rs770200551
This variant is a VUS because it does not have enough information.
552893
chr3:45434758:TAA>-
LARS2
NM_015340:c.-21-1167_-21-1165delTAA
FIVE_PRIME_INTRON
Benign
rs34525065
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
726
1322
0.5492
338
1006
0.336
266
694
0.3833
302
1008
0.2996
350
978
0.3579
1982
5008
0.395767
552895
chr3:45434759:AA>-
LARS2
NM_015340:c.-21-1166_-21-1165delAA
FIVE_PRIME_INTRON
Benign
rs58793850
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
123
1322
0.093
290
1006
0.2883
98
694
0.1412
114
1008
0.1131
181
978
0.1851
806
5008
0.160942
552896
chr3:45434829:G>A
LARS2
NM_015340:c.-21-1096G>A
FIVE_PRIME_INTRON
Unknown significance
rs566613578
This variant is a VUS because it does not have enough information.
552897
chr3:45434883:A>G
LARS2
NM_015340:c.-21-1042A>G
FIVE_PRIME_INTRON
Unknown significance
rs571953268
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
552898
chr3:45434886:G>T
LARS2
NM_015340:c.-21-1039G>T
FIVE_PRIME_INTRON
Unknown significance
rs192776556
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
552899
chr3:45434912:C>T
LARS2
NM_015340:c.-21-1013C>T
FIVE_PRIME_INTRON
Unknown significance
rs551387757
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
552900
chr3:45434981:T>C
LARS2
NM_015340:c.-21-944T>C
FIVE_PRIME_INTRON
Unknown significance
rs533745543
This variant is a VUS because it does not have enough information.
552901
chr3:45434987:A>G
LARS2
NM_015340:c.-21-938A>G
FIVE_PRIME_INTRON
Unknown significance
rs566304540
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
552902
chr3:45434997:G>A
LARS2
NM_015340:c.-21-928G>A
FIVE_PRIME_INTRON
Unknown significance
rs141788772
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
552903
chr3:45435010:T>C
LARS2
NM_015340:c.-21-915T>C
FIVE_PRIME_INTRON
Unknown significance
rs552017140
This variant is a VUS because it does not have enough information.
552904
chr3:45435031:C>T
LARS2
NM_015340:c.-21-894C>T
FIVE_PRIME_INTRON
Unknown significance
rs376302995
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
552905
chr3:45435132:T>C
LARS2
NM_015340:c.-21-793T>C
FIVE_PRIME_INTRON
Unknown significance
rs567470725
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
552906
chr3:45435145:G>C
LARS2
NM_015340:c.-21-780G>C
FIVE_PRIME_INTRON
Unknown significance
rs777051501
This variant is a VUS because it does not have enough information.
552907
chr3:45435162:G>A
LARS2
NM_015340:c.-21-763G>A
FIVE_PRIME_INTRON
Unknown significance
rs537636029
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
552908
chr3:45435175:T>C
LARS2
NM_015340:c.-21-750T>C
FIVE_PRIME_INTRON
Unknown significance
rs200050535
This variant is a VUS because it does not have enough information.
552909
chr3:45435177:G>A
LARS2
NM_015340:c.-21-748G>A
FIVE_PRIME_INTRON
Unknown significance
rs764581154
This variant is a VUS because it does not have enough information.
552910
chr3:45435179:G>T
LARS2
NM_015340:c.-21-746G>T
FIVE_PRIME_INTRON
Unknown significance
rs762567148
This variant is a VUS because it does not have enough information.
552911
chr3:45435231:G>A
LARS2
NM_015340:c.-21-694G>A
FIVE_PRIME_INTRON
Unknown significance
rs752008567
This variant is a VUS because it does not have enough information.
552912
chr3:45435251:G>A
LARS2
NM_015340:c.-21-674G>A
FIVE_PRIME_INTRON
Unknown significance
rs570433474
This variant is a VUS because it does not have enough information.
0
1322
0
2
1006
0.002
2
694
0.0029
0
1008
0
0
978
0
4
5008
0.000798722
552913
chr3:45435252:G>T
LARS2
NM_015340:c.-21-673G>T
FIVE_PRIME_INTRON
Unknown significance
rs577515462
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
1
978
0.001
2
5008
0.000399361
552914
chr3:45435257:A>G
LARS2
NM_015340:c.-21-668A>G
FIVE_PRIME_INTRON
Unknown significance
rs146951618
This variant is a VUS because it does not have enough information.
0
1322
0
1
1006
0.001
0
694
0
1
1008
0.001
3
978
0.0031
5
5008
0.000998403
552915
chr3:45435275:C>G
LARS2
NM_015340:c.-21-650C>G
FIVE_PRIME_INTRON
Unknown significance
rs766938108
This variant is a VUS because it does not have enough information.
552916
chr3:45435277:C>G
LARS2
NM_015340:c.-21-648C>G
FIVE_PRIME_INTRON
Unknown significance
rs752620721
This variant is a VUS because it does not have enough information.
552917
chr3:45435293:G>A
LARS2
NM_015340:c.-21-632G>A
FIVE_PRIME_INTRON
Unknown significance
rs553757277
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
552918
chr3:45435309:C>T
LARS2
NM_015340:c.-21-616C>T
FIVE_PRIME_INTRON
Unknown significance
rs572301519
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
552919
chr3:45435317:->A
LARS2
NM_015340:c.-21-608_-21-607insA
FIVE_PRIME_INTRON
Benign
rs557088288
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
5
1008
0.005
6
978
0.0061
11
5008
0.00219649
552920
chr3:45435320:->AAAGT
LARS2
NM_015340:c.-21-605_-21-604insAAAGT
FIVE_PRIME_INTRON
Unknown significance
rs761135216
This variant is a VUS because it does not have enough information.
552921
chr3:45435330:A>G
LARS2
NM_015340:c.-21-595A>G
FIVE_PRIME_INTRON
Unknown significance
rs543128361
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
1
694
0.0014
1
1008
0.001
0
978
0
2
5008
0.000399361
552922
chr3:45435332:A>G
LARS2
NM_015340:c.-21-593A>G
FIVE_PRIME_INTRON
Unknown significance
rs556116018
This variant is a VUS because it does not have enough information.
552923
chr3:45435378:C>T
LARS2
NM_015340:c.-21-547C>T
FIVE_PRIME_INTRON
Unknown significance
rs756062878
This variant is a VUS because it does not have enough information.
552924
chr3:45435393:T>C
LARS2
NM_015340:c.-21-532T>C
FIVE_PRIME_INTRON
Unknown significance
rs777704951
This variant is a VUS because it does not have enough information.
552925
chr3:45435410:A>G
LARS2
NM_015340:c.-21-515A>G
FIVE_PRIME_INTRON
Unknown significance
rs749135121
This variant is a VUS because it does not have enough information.
552926
chr3:45435419:G>C
LARS2
NM_015340:c.-21-506G>C
FIVE_PRIME_INTRON
Unknown significance
rs561189888
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
552927
chr3:45435424:A>G
LARS2
NM_015340:c.-21-501A>G
FIVE_PRIME_INTRON
Unknown significance
rs531966221
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
552928
chr3:45435456:T>C
LARS2
NM_015340:c.-21-469T>C
FIVE_PRIME_INTRON
Unknown significance
rs753282416
This variant is a VUS because it does not have enough information.
552929
chr3:45435488:GCCT>-
LARS2
NM_015340:c.-21-437_-21-434delGCCT
FIVE_PRIME_INTRON
Benign
rs113076915
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
49
1322
0.0371
1
1006
0.001
4
694
0.0058
0
1008
0
0
978
0
54
5008
0.0107827
552930
chr3:45435492:G>A
LARS2
NM_015340:c.-21-433G>A
FIVE_PRIME_INTRON
Unknown significance
rs544008713
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
552931
chr3:45435524:C>T
LARS2
NM_015340:c.-21-401C>T
FIVE_PRIME_INTRON
Unknown significance
rs565624366
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
552932
chr3:45435534:G>A
LARS2
NM_015340:c.-21-391G>A
FIVE_PRIME_INTRON
Unknown significance
rs374331589
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
552933
chr3:45435587:G>C
LARS2
NM_015340:c.-21-338G>C
FIVE_PRIME_INTRON
Unknown significance
rs779238581
This variant is a VUS because it does not have enough information.
552934
chr3:45435624:G>A
LARS2
NM_015340:c.-21-301G>A
FIVE_PRIME_INTRON
Unknown significance
rs183233411
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
552935
chr3:45435659:C>T
LARS2
NM_015340:c.-21-266C>T
FIVE_PRIME_INTRON
Unknown significance
rs138054777
This variant is a VUS because it does not have enough information.
1
1322
0.0008
3
1006
0.003
0
694
0
1
1008
0.001
0
978
0
5
5008
0.000998403
552936
chr3:45435660:G>A
LARS2
NM_015340:c.-21-265G>A
FIVE_PRIME_INTRON
Unknown significance
rs113221553
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
552937
chr3:45435661:C>G
LARS2
NM_015340:c.-21-264C>G
FIVE_PRIME_INTRON
Unknown significance
rs549098498
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
552938
chr3:45435682:T>C
LARS2
NM_015340:c.-21-243T>C
FIVE_PRIME_INTRON
Benign
rs114795216
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
46
1322
0.0348
0
1006
0
3
694
0.0043
0
1008
0
0
978
0
49
5008
0.00978435
552939
chr3:45435714:T>A
LARS2
NM_015340:c.-21-211T>A
FIVE_PRIME_INTRON
Unknown significance
rs537697566
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
552940
chr3:45435717:A>G
LARS2
NM_015340:c.-21-208A>G
FIVE_PRIME_INTRON
Unknown significance
rs555927937
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
552941
chr3:45435749:A>G
LARS2
NM_015340:c.-21-176A>G
FIVE_PRIME_INTRON
Unknown significance
rs571066009
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
552942
chr3:45435768:G>C
LARS2
NM_015340:c.-21-157G>C
FIVE_PRIME_INTRON
Unknown significance
rs538547443
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
552943
chr3:45435774:T>G
LARS2
NM_015340:c.-21-151T>G
FIVE_PRIME_INTRON
Unknown significance
rs754519195
This variant is a VUS because it does not have enough information.
552944
chr3:45435837:C>T
LARS2
NM_015340:c.-21-88C>T
FIVE_PRIME_INTRON
Unknown significance
rs537330594
This variant is a VUS because it does not have enough information.
552945
chr3:45435849:A>T
LARS2
NM_015340:c.-21-76A>T
FIVE_PRIME_INTRON
Benign
rs704923
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
539
1322
0.4077
50
1006
0.0497
60
694
0.0865
125
1008
0.124
65
978
0.0665
839
5008
0.167532
552946
chr3:45435878:G>A
LARS2
NM_015340:c.-21-47G>A
FIVE_PRIME_INTRON
Unknown significance
rs187923629
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
552947
chr3:45435892:A>C
LARS2
NM_015340:c.-21-33A>C
FIVE_PRIME_INTRON
Unknown significance
rs542638720
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
552948
chr3:45435902:G>A
LARS2
NM_015340:c.-21-23G>A
FIVE_PRIME_INTRON
Unknown significance
rs747550432
This variant is a VUS because it does not have enough information.
552949
chr3:45435908:T>G
LARS2
NM_015340:c.-21-17T>G
FIVE_PRIME_INTRON
Unknown significance
rs745550417
This variant is a VUS because it does not have enough information.
0
8606
0
0
9062
0
0
7096
0
0
5964
0
0
55008
0
0
774
0
1
14546
0.0000687474
1
101056
0.0000098955
552950
chr3:45435910:T>C
LARS2
NM_015340:c.-21-15T>C
FIVE_PRIME_INTRON
Unknown significance
rs757855712
This variant is a VUS because it does not have enough information.
0
8602
0
0
9106
0
0
7116
0
0
5974
0
2
55148
0.000036266
0
778
0
0
14562
0
2
101286
0.0000197461
552951
chr3:45435912:C>T
LARS2
NM_015340:c.-21-13C>T
FIVE_PRIME_INTRON
Unknown significance
rs779418705
This variant is a VUS because it does not have enough information.
0
8640
0
0
9108
0
0
7110
0
0
5988
0
1
55274
0.0000180917
0
772
0
0
14560
0
1
101452
0.00000985688
552952
chr3:45435914:C>T
LARS2
NM_015340:c.-21-11C>T
FIVE_PRIME_INTRON
Unknown significance
rs746598107
This variant is a VUS because it does not have enough information.
1
8712
0.000114784
0
9248
0
0
7160
0
0
6014
0
0
55724
0
0
784
0
2
14648
0.000136537
3
102290
0.0000293284
552953
chr3:45435916:C>G
LARS2
NM_015340:c.-21-9C>G
FIVE_PRIME_INTRON
Unknown significance
rs768447211
This variant is a VUS because it does not have enough information.
0
8748
0
1
9274
0.000107828
0
7180
0
0
6032
0
0
55988
0
0
782
0
0
14720
0
1
102724
0.00000973482
552955
chr3:45435927:C>A
LARS2
NM_015340:c.-19C>A
FIVE_PRIME_EXON
Unknown significance
rs373100137
This variant is a VUS because it does not have enough information.
0
9196
0
0
10060
0
0
7574
0
0
6240
0
1
59468
0.0000168158
0
828
0
0
15188
0
1
108554
0.00000921201
552954
chr3:45435927:C>T
LARS2
NM_015340:c.-19C>T
FIVE_PRIME_EXON
Unknown significance
rs373100137
This variant is a VUS because it does not have enough information.
0
8600
0
1
4406
0.000226963
1
13006
0.0000768876
1
9196
0.000108743
0
10060
0
0
7574
0
0
6240
0
0
59468
0
0
828
0
0
15188
0
1
108554
0.00000921201
552956
chr3:45435932:T>A
LARS2
NM_015340:c.-14T>A
FIVE_PRIME_EXON
Unknown significance
rs769746785
This variant is a VUS because it does not have enough information.
1
9552
0.00010469
0
10548
0
0
7830
0
0
6378
0
0
61736
0
0
856
0
0
15482
0
1
112382
0.00000889822
552957
chr3:45435933:C>T
LARS2
NM_015340:c.-13C>T
FIVE_PRIME_EXON
Unknown significance
rs774651149
This variant is a VUS because it does not have enough information.
1
9594
0.000104232
0
10624
0
0
7862
0
0
6394
0
0
62136
0
0
860
0
0
15538
0
1
113008
0.00000884893
552958
chr3:45435934:A>G
LARS2
NM_015340:c.-12A>G
FIVE_PRIME_EXON
Unknown significance
rs759694320
This variant is a VUS because it does not have enough information.
0
9662
0
1
10732
0.0000931793
2
7910
0.000252845
0
6426
0
0
62590
0
0
864
0
0
15608
0
3
113792
0.0000263639
552959
chr3:45435940:T>A
LARS2
NM_015340:c.-6T>A
FIVE_PRIME_EXON
Unknown significance
rs767835303
This variant is a VUS because it does not have enough information.
0
9880
0
0
11062
0
0
8138
0
1
6512
0.000153563
2
64352
0.0000310791
0
878
0
0
15884
0
3
116706
0.0000257056
552960
chr3:45435943:A>G
LARS2
NM_015340:c.-3A>G
FIVE_PRIME_EXON
Unknown significance
rs775423833
This variant is a VUS because it does not have enough information.
0
9990
0
0
11164
0
0
8258
0
0
6548
0
1
64994
0.000015386
0
888
0
0
15998
0
1
117840
0.00000848608
552961
chr3:45435955:G>A
LARS2
NM_015340:p.Val4Ile
NM_015340:c.10G>A
EXON3
Likely benign
rs760845178
Pathogenicity is based on prediction data only. 1 out of 6 predictions were pathogenic.
-0.843
N
0.135;0.135;0.035;0.13;0.153
T;T;D;T;T
0.008
B
0.506386
N
1
N
-5.05
N
0
10290
0
0
11436
0
1
8526
0.000117288
0
6596
0
0
66236
0
0
900
0
0
16318
0
1
120302
0.00000831241
552962
chr3:45435967:T>C
LARS2
NM_015340:p.Leu8Leu
NM_015340:c.22T>C
EXON3
Benign
rs77377258
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
1
8600
0.000116279
87
4406
0.0197458
88
13006
0.00676611
38
1322
0.0287
0
1006
0
0
694
0
0
1008
0
0
978
0
38
5008
0.00758786
212
10374
0.0204357
10
11518
0.000868206
0
8626
0
0
6610
0
9
66608
0.000135119
0
906
0
2
16446
0.00012161
233
121088
0.00192422
552963
chr3:45435983:C>T
LARS2
NM_015340:p.Ser13Phe
NM_015340:c.38C>T
EXON3
Likely benign
rs754363894
Pathogenicity is based on prediction data only. 2 out of 6 predictions were pathogenic.
-0.007
N
0.008;0.008;0.04;0.007;0.051
D;D;D;D;T
0.641;0.412
P;B
0.394181
N
1
N
-0.379
N
0
10398
0
0
11558
0
0
8650
0
0
6614
0
2
66718
0.0000299769
0
908
0
0
16494
0
2
121340
0.0000164826
552964
chr3:45435987:T>C
LARS2
NM_015340:p.Leu14Leu
NM_015340:c.42T>C
EXON3
Unknown significance
rs200517209
This variant is a VUS because it does not have enough information.
0
10400
0
0
11560
0
0
8652
0
0
6614
0
2
66718
0.0000299769
0
908
0
0
16500
0
2
121352
0.000016481
552965
chr3:45436000:C>G
LARS2
NM_015340:p.Leu19Val
NM_015340:c.55C>G
EXON3
Unknown significance
rs765588082
This variant is a VUS because it does not have enough information.
0.007
N
0.0;0.0;0.0;0.0;0.007
D
0.999;0.997
D
0.015218
N
0.801544
N
3.25
C
0
10406
0
0
11572
0
0
8654
0
0
6614
0
1
66730
0.0000149858
0
908
0
1
16510
0.0000605694
2
121394
0.0000164753
552966
chr3:45436025:A>C
LARS2
NM_015340:p.Lys27Thr
NM_015340:c.80A>C
EXON3
Likely benign
rs776961881
Pathogenicity is based on prediction data only. 0 out of 6 predictions were pathogenic.
-0.832
N
0.482;0.482;0.095;0.469;0.517
T
0.0
B
0.106154
N
1
N
-7.39
N
552967
chr3:45436026:G>C
LARS2
NM_015340:p.Lys27Asn
NM_015340:c.81G>C
EXON3
Likely benign
rs146378764
Pathogenicity is based on prediction data only. 0 out of 6 predictions were pathogenic.
0.031
N
0.511;0.511;0.298;0.508;0.527
T
0.0
B
0.106154
N
1
N
-6.0
N
0
8600
0
1
4406
0.000226963
1
13006
0.0000768876
3
10406
0.000288295
0
11576
0
0
8654
0
0
6614
0
0
66734
0
0
908
0
0
16510
0
3
121402
0.0000247113
552968
chr3:45436034:G>A
LARS2
NM_015340:p.Arg30Lys
NM_015340:c.89G>A
EXON3
Likely benign
rs752704499
Pathogenicity is based on prediction data only. 1 out of 6 predictions were pathogenic.
0.722
N
0.319;0.319;0.196;0.319;0.246
T
0.0
B
0.171991
N
1
N
1.99
C
0
10406
0
0
11578
0
0
8654
0
1
6614
0.000151194
4
66732
0.0000599413
0
908
0
0
16510
0
5
121402
0.0000411855
552969
chr3:45436043:T>C
LARS2
NM_015340:p.Ile33Thr
NM_015340:c.98T>C
EXON3
Likely benign
rs779796862
Pathogenicity is based on prediction data only. 1 out of 6 predictions were pathogenic.
0.084
N
0.038;0.038;0.005;0.054;0.151
D;D;D;T;T
0.146;0.085
B
0.680492
N
1
N
-4.92
N
0
10406
0
0
11578
0
0
8654
0
0
6614
0
3
66734
0.0000449546
0
908
0
0
16510
0
3
121404
0.0000247109
552970
chr3:45436048:G>A
LARS2
NM_015340:p.Gly35Arg
NM_015340:c.103G>A
EXON3
Likely benign
rs113559893
Pathogenicity is based on prediction data only. 1 out of 6 predictions were pathogenic.
-0.974
N
0.458;0.458;0.234;0.257;0.284
T
0.042;0.019
B
0.247383
N
1
N
2.21
C
1
8600
0.000116279
0
4406
0
1
13006
0.0000768876
552971
chr3:45436068:C>T
LARS2
NM_015340:p.Tyr41Tyr
NM_015340:c.123C>T
EXON3
Unknown significance
rs751011983
This variant is a VUS because it does not have enough information.
0
10406
0
1
11578
0.0000863707
0
8654
0
0
6614
0
0
66728
0
0
908
0
0
16510
0
1
121398
0.00000823737
552972
chr3:45436069:A>G
LARS2
NM_015340:p.Ser42Gly
NM_015340:c.124A>G
EXON3
Unknown significance
rs373693561
This variant is a VUS because it does not have enough information.
1.088
C
0.012;0.012;0.002;0.0;0.01
D
0.997
D
0
D
0.999983
D;D
5.04
C
0
10406
0
0
11578
0
0
8654
0
0
6614
0
1
66728
0.0000149862
0
908
0
0
16510
0
1
121398
0.00000823737
552973
chr3:45436076:C>T
LARS2
NM_015340:p.Thr44Met
NM_015340:c.131C>T
EXON3
Unknown significance
rs781238503
This variant is a VUS because it does not have enough information.
0.013
N
0.002;0.002;0.0;0.001;0.001
D
1.0
D
0.000001
D
0.999962
D;D
4.17
C
0
10402
0
0
11576
0
1
8650
0.000115607
0
6614
0
0
66718
0
0
908
0
0
16508
0
1
121376
0.00000823886
552974
chr3:45436077:G>-
LARS2
NM_015340:c.132delG
EXON3
Unknown significance
rs776107034
This variant is a VUS because it does not have enough information.
0
10402
0
0
11576
0
2
8650
0.000231214
0
6614
0
0
66718
0
0
908
0
0
16508
0
2
121376
0.0000164777
552975
chr3:45436077:G>A
LARS2
NM_015340:p.Thr44Thr
NM_015340:c.132G>A
EXON3
Unknown significance
rs576608165
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
0
10404
0
1
11578
0.0000863707
0
8646
0
0
6614
0
1
66718
0.0000149885
0
908
0
3
16508
0.00018173
5
121376
0.0000411943
552976
chr3:45436080:A>T
LARS2
NM_015340:p.Gly45Gly
NM_015340:c.135A>T
EXON3
Unknown significance
rs143095137
This variant is a VUS because it does not have enough information.
0
8600
0
2
4406
0.000453926
2
13006
0.000153775
3
10398
0.000288517
0
11578
0
0
8650
0
0
6614
0
0
66710
0
0
908
0
0
16506
0
3
121364
0.000024719
552977
chr3:45436090:A>G
LARS2
NM_015340:p.Lys49Glu
NM_015340:c.145A>G
EXON3
Unknown significance
rs777694670
This variant is a VUS because it does not have enough information.
1.088
C
0.142;0.142;0.001;0.005;0.194
T;T;D;D;T
0.297
B
0.000718
D
0.968441
D;D
5.04
C
0
10396
0
0
11578
0
0
8648
0
0
6614
0
1
66698
0.000014993
0
908
0
0
16506
0
1
121348
0.00000824076
552978
chr3:45436093:G>A
LARS2
NM_015340:p.Glu50Lys
NM_015340:c.148G>A
EXON3
Unknown significance
rs200135115
This variant is a VUS because it does not have enough information.
0.953
C
0.365;0.365;0.188;0.294;0.141
T
0.0
B
0.049015
N
0.899357
D;N
4.16
C
0
1322
0
0
1006
0
0
694
0
1
1008
0.001
0
978
0
1
5008
0.000199681
0
10396
0
0
11578
0
7
8648
0.000809436
0
6614
0
0
66694
0
0
908
0
0
16506
0
7
121344
0.0000576872
552979
chr3:45436101:A>G
LARS2
NM_015340:p.Thr52Thr
NM_015340:c.156A>G
EXON3
Unknown significance
rs772150626
This variant is a VUS because it does not have enough information.
0
10390
0
0
11576
0
0
8648
0
0
6614
0
0
66680
0
0
908
0
2
16506
0.000121168
2
121322
0.0000164851
552980
chr3:45436101:A>T
LARS2
NM_015340:p.Thr52Thr
NM_015340:c.156A>T
EXON3
Unknown significance
rs772150626
This variant is a VUS because it does not have enough information.
0
10390
0
0
11576
0
0
8648
0
0
6614
0
1
66680
0.000014997
0
908
0
0
16506
0
1
121322
0.00000824253
552981
chr3:45436102:T>C
LARS2
NM_015340:p.Leu53Leu
NM_015340:c.157T>C
EXON3
Benign
rs141607519
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
4
8600
0.000465116
9
4406
0.00204267
13
13006
0.000999539
0
1322
0
0
1006
0
32
694
0.0461
0
1008
0
0
978
0
32
5008
0.00638978
16
10388
0.00154024
1426
11576
0.123186
0
8648
0
0
6614
0
9
66680
0.000134973
6
908
0.00660793
0
16506
0
1457
121320
0.0120096
552982
chr3:45436114:A>G
LARS2
NM_015340:p.Lys57Glu
NM_015340:c.169A>G
EXON3
Unknown significance
rs768754426
This variant is a VUS because it does not have enough information.
1.088
C
0.104;0.104;0.004;0.036;0.088
T;T;D;D;T
0.651
P
0.004195
N
0.866042
D;N
5.04
C
0
10386
0
0
11570
0
1
8646
0.00011566
0
6614
0
0
66654
0
0
906
0
0
16500
0
1
121276
0.00000824565
552983
chr3:45436117:G>A
LARS2
NM_015340:p.Asp58Asn
NM_015340:c.172G>A
EXON3
Likely benign
rs777055524
Pathogenicity is based on prediction data only. 2 out of 6 predictions were pathogenic.
0.953
C
0.271;0.271;0.068;0.18;0.333
T
0.094;0.183
B
0.014035
N
0.985181
N;N;N
4.15
C
0
10384
0
0
11570
0
0
8646
0
0
6612
0
1
66650
0.0000150038
0
906
0
0
16500
0
1
121268
0.0000082462
552984
chr3:45436124:A>G
LARS2
NM_015340:p.Glu60Gly
NM_015340:c.179A>G
EXON3
Unknown significance
rs762319941
This variant is a VUS because it does not have enough information.
1.088
C
0.001;0.001;0.006;0.0;0.0
D
1.0
D
0
D
1
D;D
5.04
C
0
10380
0
0
11568
0
0
8646
0
0
6612
0
0
66640
0
0
906
0
1
16500
0.0000606061
1
121252
0.00000824729
552985
chr3:45436125:G>C
LARS2
NM_015340:p.Glu60Asp
NM_015340:c.180G>C
EXON3
Unknown significance
rs199568924
This variant is a VUS because it does not have enough information.
0.953
C
0.006;0.006;0.007;0.0;0.0
D
0.999;1.0
D
0
D
0.999992
D;D
3.91
C
0
10380
0
0
11564
0
0
8646
0
0
6612
0
10
66636
0.000150069
0
906
0
0
16500
0
10
121244
0.0000824783
552986
chr3:45436142:G>A
LARS2
NM_015340:p.Arg66Gln
NM_015340:c.197G>A
EXON3
Likely benign
rs149789249
Pathogenicity is based on prediction data only. 1 out of 6 predictions were pathogenic.
0.091
N
0.618;0.618;0.121;0.121;0.302
T
0.272;0.447
B
0.001648
N
0.999973
N;N
3.22
C
1
8600
0.000116279
0
4406
0
1
13006
0.0000768876
552987
chr3:45436147:A>G
LARS2
NM_015340:p.Lys68Glu
NM_015340:c.202A>G
EXON3
Unknown significance
rs553596357
This variant is a VUS because it does not have enough information.
1.088
C
0.536;0.536;0.012;0.047;0.131
T;T;D;D;T
0.22;0.379
B
0.000008
D
0.513918
N;N
2.48
C
552988
chr3:45436153:C>T
LARS2
NM_015340:p.Gln70Stop
NM_015340:c.208C>T
EXON3
Unknown significance
rs750723957
This variant is a VUS because it does not have enough information.
0.852
N
0.009835
N
1
A
3.11
C
0
10278
0
0
11542
0
0
8638
0
0
6606
0
0
66496
0
0
904
0
1
16482
0.0000606722
1
120946
0.00000826815
552989
chr3:45436158:C>T
LARS2
NM_015340:p.Ala71Ala
NM_015340:c.213C>T
EXON3
Unknown significance
rs763424959
This variant is a VUS because it does not have enough information.
0
10262
0
0
11542
0
0
8636
0
0
6606
0
1
66452
0.0000150485
0
906
0
0
16452
0
1
120856
0.00000827431
552990
chr3:45436160:C>T
LARS2
NM_015340:p.Ser72Phe
NM_015340:c.215C>T
EXON3
Likely benign
rs532725261
Pathogenicity is based on prediction data only. 0 out of 6 predictions were pathogenic.
0.852
N
0.694;0.694;0.602;0.678;0.722
T
0.001;0.0
B
0.648334
N
1
N
-1.75
N
0
1322
0
0
1006
0
0
694
0
0
1008
0
4
978
0.0041
4
5008
0.000798722
0
10256
0
0
11544
0
0
8624
0
0
6606
0
1
66434
0.0000150525
0
904
0
35
16448
0.00212792
36
120816
0.000297974
552991
chr3:45436161:C>T
LARS2
NM_015340:p.Ser72Ser
NM_015340:c.216C>T
EXON3
Unknown significance
rs751261319
This variant is a VUS because it does not have enough information.
0
10244
0
0
11540
0
1
8626
0.000115929
0
6606
0
0
66414
0
0
904
0
0
16440
0
1
120774
0.00000827993
552992
chr3:45436164:A>G
LARS2
NM_015340:p.Lys73Lys
NM_015340:c.219A>G
EXON3
Unknown significance
rs754475523
This variant is a VUS because it does not have enough information.
0
10240
0
2
11538
0.00017334
0
8620
0
0
6606
0
0
66394
0
0
902
0
0
16436
0
2
120736
0.0000165651
552993
chr3:45436165:A>G
LARS2
NM_015340:p.Ile74Val
NM_015340:c.220A>G
EXON3
Likely benign
rs780865850
Pathogenicity is based on prediction data only. 0 out of 6 predictions were pathogenic.
-0.2
N
0.364;0.364;0.268;0.247;0.481
T
0.001;0.0
B
0.657487
N
1
N
-2.09
N
0
10232
0
3
11534
0.000260101
0
8608
0
0
6606
0
0
66364
0
0
902
0
0
16426
0
3
120672
0.0000248608
552994
chr3:45436169:C>T
LARS2
NM_015340:p.Ser75Leu
NM_015340:c.224C>T
EXON3
Unknown significance
rs541763978
This variant is a VUS because it does not have enough information.
0.852
N
0.128;0.128;0.002;0.012;0.04
T;T;D;D;D
0.801
P
0.112176
N
0.999999
N;N
4.16
C
0
1322
0
0
1006
0
0
694
0
0
1008
0
1
978
0.001
1
5008
0.000199681
0
10192
0
0
11526
0
0
8590
0
0
6604
0
0
66250
0
0
900
0
2
16388
0.000122041
2
120450
0.0000166044
552995
chr3:45436183:A>C
LARS2
NM_015340:c.234+4A>C
INTRON3
Unknown significance
rs370289532
This variant is a VUS because it does not have enough information.
1
8600
0.000116279
0
4406
0
1
13006
0.0000768876
0
10012
0
0
11442
0
0
8426
0
0
6594
0
4
65500
0.0000610687
0
896
0
0
16122
0
4
118992
0.0000336157
552996
chr3:45436196:A>G
LARS2
NM_015340:c.234+17A>G
INTRON3
Unknown significance
rs777894830
This variant is a VUS because it does not have enough information.
0
9812
0
0
11314
0
0
8266
0
0
6582
0
0
64652
0
1
894
0.00111857
1
15790
0.0000633312
2
117310
0.0000170488
552997
chr3:45436197:T>G
LARS2
NM_015340:c.234+18T>G
INTRON3
Unknown significance
rs376300134
This variant is a VUS because it does not have enough information.
0
8600
0
3
4406
0.00068089
3
13006
0.000230663
4
9794
0.000408413
0
11308
0
0
8250
0
0
6580
0
0
64570
0
0
892
0
0
15776
0
4
117170
0.0000341384
552998
chr3:45436199:C>T
LARS2
NM_015340:c.234+20C>T
INTRON3
Unknown significance
rs770781729
This variant is a VUS because it does not have enough information.
2
9752
0.000205086
0
11286
0
0
8214
0
0
6576
0
0
64376
0
0
888
0
0
15730
0
2
116822
0.0000171201
552999
chr3:45436202:A>G
LARS2
NM_015340:c.234+23A>G
INTRON3
Unknown significance
rs780098894
This variant is a VUS because it does not have enough information.
1
9690
0.000103199
0
11238
0
0
8158
0
0
6572
0
0
64166
0
0
886
0
0
15652
0
1
116362
0.00000859387
553000
chr3:45436203:G>A
LARS2
NM_015340:c.234+24G>A
INTRON3
Unknown significance
rs74724761
This variant is a VUS because it does not have enough information.
553001
chr3:45436204:A>G
LARS2
NM_015340:c.234+25A>G
INTRON3
Unknown significance
rs747258634
This variant is a VUS because it does not have enough information.
1
9690
0.000103199
1
11224
0.0000890948
0
8132
0
0
6568
0
2
64054
0.0000312237
0
886
0
0
15640
0
4
116194
0.0000344252
553002
chr3:45436207:G>T
LARS2
NM_015340:c.234+28G>T
INTRON3
Unknown significance
rs768664426
This variant is a VUS because it does not have enough information.
1
9664
0.000103477
0
11194
0
0
8088
0
0
6562
0
0
63916
0
0
888
0
0
15576
0
1
115888
0.00000862902
553003
chr3:45436213:A>G
LARS2
NM_015340:c.234+34A>G
INTRON3
Unknown significance
rs758150360
This variant is a VUS because it does not have enough information.
0
9590
0
0
11162
0
0
8016
0
0
6560
0
4
63600
0.0000628931
0
886
0
0
15498
0
4
115312
0.0000346885
553004
chr3:45436218:G>A
LARS2
NM_015340:c.234+39G>A
INTRON3
Unknown significance
rs761923130
This variant is a VUS because it does not have enough information.
0
9530
0
0
11094
0
0
7922
0
0
6544
0
1
63068
0.0000158559
0
874
0
0
15356
0
1
114388
0.00000874218
553005
chr3:45436218:G>C
LARS2
NM_015340:c.234+39G>C
INTRON3
Unknown significance
rs761923130
This variant is a VUS because it does not have enough information.
0
9530
0
0
11094
0
0
7922
0
0
6544
0
1
63068
0.0000158559
0
874
0
0
15356
0
1
114388
0.00000874218
553006
chr3:45436219:G>A
LARS2
NM_015340:c.234+40G>A
INTRON3
Unknown significance
rs773791700
This variant is a VUS because it does not have enough information.
0
9502
0
0
11046
0
1
7900
0.000126582
0
6542
0
0
62904
0
0
874
0
0
15290
0
1
114058
0.00000876747
553007
chr3:45436219:G>C
LARS2
NM_015340:c.234+40G>C
INTRON3
Unknown significance
rs773791700
This variant is a VUS because it does not have enough information.
0
9502
0
0
11046
0
0
7900
0
0
6542
0
1
62904
0.0000158972
0
874
0
0
15290
0
1
114058
0.00000876747
553008
chr3:45436220:G>C
LARS2
NM_015340:c.234+41G>C
INTRON3
Unknown significance
rs766775824
This variant is a VUS because it does not have enough information.
2
9506
0.000210393
0
11052
0
0
7890
0
0
6536
0
0
62920
0
0
874
0
0
15288
0
2
114066
0.0000175337
553009
chr3:45436225:A>G
LARS2
NM_015340:c.234+46A>G
INTRON3
Benign
rs41289596
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
51
8598
0.00593161
6
4404
0.0013624
57
13002
0.00438394
0
1322
0
5
1006
0.005
0
694
0
0
1008
0
3
978
0.0031
8
5008
0.00159744
11
9444
0.00116476
9
10900
0.000825688
0
7818
0
31
6522
0.00475314
292
62332
0.00468459
4
870
0.0045977
36
15118
0.00238127
383
113004
0.00338926
553010
chr3:45436227:GTT>-
LARS2
NM_015340:c.234+48_234+50delGTT
INTRON3
Unknown significance
rs373212405
This variant is a VUS because it does not have enough information.
553011
chr3:45436229:T>C
LARS2
NM_015340:c.234+50T>C
INTRON3
Unknown significance
rs759252058
This variant is a VUS because it does not have enough information.
0
9356
0
0
10776
0
1
7738
0.000129232
0
6514
0
0
61722
0
0
858
0
0
14920
0
1
111884
0.00000893783
553012
chr3:45436232:->AA
LARS2
NM_015340:c.234+53_234+54insAA
INTRON3
Unknown significance
rs746549970
This variant is a VUS because it does not have enough information.
553013
chr3:45436234:CCCT>-
LARS2
NM_015340:c.234+55_234+58delCCCT
INTRON3
Unknown significance
rs376371040
This variant is a VUS because it does not have enough information.
553014
chr3:45436276:G>-
LARS2
NM_015340:c.234+97delG
INTRON3
Unknown significance
rs367627685
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
553015
chr3:45436376:A>G
LARS2
NM_015340:c.234+197A>G
INTRON3
Unknown significance
rs752215444
This variant is a VUS because it does not have enough information.
553016
chr3:45436380:G>T
LARS2
NM_015340:c.234+201G>T
INTRON3
Unknown significance
rs117629080
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
553017
chr3:45436385:G>T
LARS2
NM_015340:c.234+206G>T
INTRON3
Unknown significance
rs367604121
This variant is a VUS because it does not have enough information.
553018
chr3:45436413:T>C
LARS2
NM_015340:c.234+234T>C
INTRON3
Unknown significance
rs760629680
This variant is a VUS because it does not have enough information.
553019
chr3:45436415:G>A
LARS2
NM_015340:c.234+236G>A
INTRON3
Unknown significance
rs548701154
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
553020
chr3:45436416:T>C
LARS2
NM_015340:c.234+237T>C
INTRON3
Benign
rs561081543
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
7
1322
0.0053
0
1006
0
0
694
0
0
1008
0
0
978
0
7
5008
0.00139776
553021
chr3:45436435:T>G
LARS2
NM_015340:c.234+256T>G
INTRON3
Benign
rs150510168
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
12
1322
0.0091
0
1006
0
0
694
0
0
1008
0
0
978
0
12
5008
0.00239617
553022
chr3:45436451:A>G
LARS2
NM_015340:c.234+272A>G
INTRON3
Unknown significance
rs372293755
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
553023
chr3:45436458:T>C
LARS2
NM_015340:c.234+279T>C
INTRON3
Unknown significance
rs571128774
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
553024
chr3:45436464:G>A
LARS2
NM_015340:c.234+285G>A
INTRON3
Unknown significance
rs538414382
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
553025
chr3:45436467:C>T
LARS2
NM_015340:c.234+288C>T
INTRON3
Unknown significance
rs764074451
This variant is a VUS because it does not have enough information.
553026
chr3:45436473:G>A
LARS2
NM_015340:c.234+294G>A
INTRON3
Benign
rs17637580
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
136
1322
0.1029
290
1006
0.2883
98
694
0.1412
114
1008
0.1131
181
978
0.1851
819
5008
0.163538
553027
chr3:45436505:G>C
LARS2
NM_015340:c.234+326G>C
INTRON3
Unknown significance
rs138628716
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
553028
chr3:45436571:C>T
LARS2
NM_015340:c.234+392C>T
INTRON3
Unknown significance
rs149327667
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
553029
chr3:45436585:G>A
LARS2
NM_015340:c.234+406G>A
INTRON3
Benign
rs191911157
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
16
1322
0.0121
0
1006
0
1
694
0.0014
0
1008
0
0
978
0
17
5008
0.00339457
553030
chr3:45436591:C>G
LARS2
NM_015340:c.234+412C>G
INTRON3
Unknown significance
rs576796235
This variant is a VUS because it does not have enough information.
553031
chr3:45436592:A>G
LARS2
NM_015340:c.234+413A>G
INTRON3
Benign
rs116639712
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
24
1322
0.0182
0
1006
0
1
694
0.0014
0
1008
0
0
978
0
25
5008
0.00499201
553032
chr3:45436623:C>A
LARS2
NM_015340:c.234+444C>A
INTRON3
Unknown significance
rs374183907
This variant is a VUS because it does not have enough information.
553033
chr3:45436681:C>G
LARS2
NM_015340:c.234+502C>G
INTRON3
Unknown significance
rs778866778
This variant is a VUS because it does not have enough information.
553034
chr3:45436691:C>T
LARS2
NM_015340:c.234+512C>T
INTRON3
Unknown significance
rs750647709
This variant is a VUS because it does not have enough information.
553035
chr3:45436700:C>T
LARS2
NM_015340:c.234+521C>T
INTRON3
Unknown significance
rs367665199
This variant is a VUS because it does not have enough information.
553036
chr3:45436795:A>G
LARS2
NM_015340:c.234+616A>G
INTRON3
Unknown significance
rs758617576
This variant is a VUS because it does not have enough information.
553037
chr3:45436805:G>T
LARS2
NM_015340:c.234+626G>T
INTRON3
Unknown significance
rs537564172
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
553038
chr3:45436850:C>T
LARS2
NM_015340:c.234+671C>T
INTRON3
Benign
rs559057997
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
5
978
0.0051
5
5008
0.000998403
553039
chr3:45436851:C>T
LARS2
NM_015340:c.234+672C>T
INTRON3
Unknown significance
rs747111956
This variant is a VUS because it does not have enough information.
553040
chr3:45436913:C>T
LARS2
NM_015340:c.234+734C>T
INTRON3
Unknown significance
rs577546762
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
553041
chr3:45436941:A>C
LARS2
NM_015340:c.234+762A>C
INTRON3
Benign
rs17077759
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
243
1322
0.1838
186
1006
0.1849
98
694
0.1412
7
1008
0.0069
140
978
0.1431
674
5008
0.134585
553042
chr3:45437037:G>A
LARS2
NM_015340:c.234+858G>A
INTRON3
Unknown significance
rs781632664
This variant is a VUS because it does not have enough information.
553043
chr3:45437064:G>-
LARS2
NM_015340:c.234+885delG
INTRON3
Unknown significance
rs757693519
This variant is a VUS because it does not have enough information.
553044
chr3:45437182:A>G
LARS2
NM_015340:c.234+1003A>G
INTRON3
Unknown significance
rs560039463
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
553045
chr3:45437185:T>-
LARS2
NM_015340:c.234+1006delT
INTRON3
Unknown significance
rs781399779
This variant is a VUS because it does not have enough information.
553046
chr3:45437193:C>T
LARS2
NM_015340:c.234+1014C>T
INTRON3
Unknown significance
rs575020488
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
553047
chr3:45437198:A>-
LARS2
NM_015340:c.234+1019delA
INTRON3
Unknown significance
rs578002503
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
553048
chr3:45437206:C>G
LARS2
NM_015340:c.234+1027C>G
INTRON3
Unknown significance
rs78292795
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
553049
chr3:45437222:T>C
LARS2
NM_015340:c.234+1043T>C
INTRON3
Benign
rs146282435
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
7
1322
0.0053
0
1006
0
1
694
0.0014
0
1008
0
0
978
0
8
5008
0.00159744
553050
chr3:45437224:G>C
LARS2
NM_015340:c.234+1045G>C
INTRON3
Unknown significance
rs531181989
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
553051
chr3:45437324:T>A
LARS2
NM_015340:c.234+1145T>A
INTRON3
Unknown significance
rs549483147
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
553052
chr3:45437345:T>A
LARS2
NM_015340:c.234+1166T>A
INTRON3
Unknown significance
rs770083821
This variant is a VUS because it does not have enough information.
553053
chr3:45437351:G>A
LARS2
NM_015340:c.234+1172G>A
INTRON3
Unknown significance
rs564624575
This variant is a VUS because it does not have enough information.
3
1322
0.0023
1
1006
0.001
0
694
0
0
1008
0
0
978
0
4
5008
0.000798722
553054
chr3:45437359:G>A
LARS2
NM_015340:c.234+1180G>A
INTRON3
Unknown significance
rs532203634
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
0
694
0
0
1008
0
4
978
0.0041
4
5008
0.000798722
553055
chr3:45437372:T>C
LARS2
NM_015340:c.234+1193T>C
INTRON3
Benign
rs139279474
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
5
1008
0.005
0
978
0
5
5008
0.000998403
553056
chr3:45437392:T>C
LARS2
NM_015340:c.234+1213T>C
INTRON3
Unknown significance
rs773505005
This variant is a VUS because it does not have enough information.
553057
chr3:45437405:T>G
LARS2
NM_015340:c.234+1226T>G
INTRON3
Unknown significance
rs532045690
This variant is a VUS because it does not have enough information.
553058
chr3:45437408:A>C
LARS2
NM_015340:c.234+1229A>C
INTRON3
Unknown significance
rs759221706
This variant is a VUS because it does not have enough information.
553059
chr3:45437433:T>G
LARS2
NM_015340:c.234+1254T>G
INTRON3
Benign
rs374943577
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
5
1008
0.005
6
978
0.0061
11
5008
0.00219649
553060
chr3:45437455:T>C
LARS2
NM_015340:c.234+1276T>C
INTRON3
Benign
rs184336723
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
6
1008
0.006
0
978
0
6
5008
0.00119808
553061
chr3:45437465:T>C
LARS2
NM_015340:c.234+1286T>C
INTRON3
Unknown significance
rs745871935
This variant is a VUS because it does not have enough information.
553062
chr3:45437512:G>A
LARS2
NM_015340:c.234+1333G>A
INTRON3
Unknown significance
rs368452536
This variant is a VUS because it does not have enough information.
553063
chr3:45437530:T>C
LARS2
NM_015340:c.234+1351T>C
INTRON3
Unknown significance
rs548436756
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
553064
chr3:45437534:T>C
LARS2
NM_015340:c.234+1355T>C
INTRON3
Unknown significance
rs771662093
This variant is a VUS because it does not have enough information.
553065
chr3:45437542:G>A
LARS2
NM_015340:c.234+1363G>A
INTRON3
Unknown significance
rs769935697
This variant is a VUS because it does not have enough information.
553066
chr3:45437581:G>A
LARS2
NM_015340:c.234+1402G>A
INTRON3
Unknown significance
rs775042609
This variant is a VUS because it does not have enough information.
553067
chr3:45437686:T>C
LARS2
NM_015340:c.234+1507T>C
INTRON3
Unknown significance
rs188426241
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
553068
chr3:45437693:C>T
LARS2
NM_015340:c.234+1514C>T
INTRON3
Benign
rs192732191
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
6
1008
0.006
0
978
0
6
5008
0.00119808
553069
chr3:45437735:T>C
LARS2
NM_015340:c.234+1556T>C
INTRON3
Unknown significance
rs760064401
This variant is a VUS because it does not have enough information.
553070
chr3:45437752:A>G
LARS2
NM_015340:c.234+1573A>G
INTRON3
Unknown significance
rs763702061
This variant is a VUS because it does not have enough information.
553071
chr3:45437794:G>T
LARS2
NM_015340:c.234+1615G>T
INTRON3
Unknown significance
rs559120327
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
553072
chr3:45437797:G>A
LARS2
NM_015340:c.234+1618G>A
INTRON3
Unknown significance
rs753772837
This variant is a VUS because it does not have enough information.
553073
chr3:45437805:C>T
LARS2
NM_015340:c.234+1626C>T
INTRON3
Unknown significance
rs761902065
This variant is a VUS because it does not have enough information.
553074
chr3:45437853:C>T
LARS2
NM_015340:c.234+1674C>T
INTRON3
Unknown significance
rs371811402
This variant is a VUS because it does not have enough information.
553075
chr3:45437865:C>A
LARS2
NM_015340:c.234+1686C>A
INTRON3
Unknown significance
rs775816270
This variant is a VUS because it does not have enough information.
553076
chr3:45437885:T>G
LARS2
NM_015340:c.234+1706T>G
INTRON3
Benign
rs144120465
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
553077
chr3:45437895:A>G
LARS2
NM_015340:c.234+1716A>G
INTRON3
Unknown significance
rs535259263
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
553078
chr3:45437973:A>G
LARS2
NM_015340:c.234+1794A>G
INTRON3
Unknown significance
rs375438685
This variant is a VUS because it does not have enough information.
553079
chr3:45437974:C>T
LARS2
NM_015340:c.234+1795C>T
INTRON3
Unknown significance
rs562107271
This variant is a VUS because it does not have enough information.
553080
chr3:45437988:C>G
LARS2
NM_015340:c.234+1809C>G
INTRON3
Unknown significance
rs553297399
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
553081
chr3:45438006:C>T
LARS2
NM_015340:c.234+1827C>T
INTRON3
Benign
rs17077760
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
49
1322
0.0371
1
1006
0.001
4
694
0.0058
0
1008
0
0
978
0
54
5008
0.0107827
553082
chr3:45438021:T>G
LARS2
NM_015340:c.234+1842T>G
INTRON3
Unknown significance
rs370017397
This variant is a VUS because it does not have enough information.
553083
chr3:45438141:C>T
LARS2
NM_015340:c.234+1962C>T
INTRON3
Benign
rs854192
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
574
1322
0.4342
190
1006
0.1889
120
694
0.1729
7
1008
0.0069
139
978
0.1421
1030
5008
0.205671
553084
chr3:45438146:A>G
LARS2
NM_015340:c.234+1967A>G
INTRON3
Unknown significance
rs563607364
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
553085
chr3:45438171:C>T
LARS2
NM_015340:c.234+1992C>T
INTRON3
Unknown significance
rs575668424
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
553086
chr3:45438181:C>G
LARS2
NM_015340:c.234+2002C>G
INTRON3
Unknown significance
rs780094700
This variant is a VUS because it does not have enough information.
553087
chr3:45438192:C>A
LARS2
NM_015340:c.234+2013C>A
INTRON3
Unknown significance
rs751834389
This variant is a VUS because it does not have enough information.
553088
chr3:45438217:C>G
LARS2
NM_015340:c.234+2038C>G
INTRON3
Unknown significance
rs371782142
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
553089
chr3:45438218:G>A
LARS2
NM_015340:c.234+2039G>A
INTRON3
Unknown significance
rs774843159
This variant is a VUS because it does not have enough information.
553090
chr3:45438251:G>T
LARS2
NM_015340:c.234+2072G>T
INTRON3
Unknown significance
rs75405540
This variant is a VUS because it does not have enough information.
553091
chr3:45438266:G>A
LARS2
NM_015340:c.234+2087G>A
INTRON3
Unknown significance
rs13091602
This variant is a VUS because it does not have enough information.
553092
chr3:45438281:A>G
LARS2
NM_015340:c.234+2102A>G
INTRON3
Unknown significance
rs754980706
This variant is a VUS because it does not have enough information.
553093
chr3:45438305:A>C
LARS2
NM_015340:c.234+2126A>C
INTRON3
Benign
rs564686552
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
553094
chr3:45438375:C>T
LARS2
NM_015340:c.234+2196C>T
INTRON3
Benign
rs148537243
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
5
694
0.0072
0
1008
0
14
978
0.0143
32
5008
0.00638978
553095
chr3:45438377:C>A
LARS2
NM_015340:c.234+2198C>A
INTRON3
Unknown significance
rs748638604
This variant is a VUS because it does not have enough information.
553096
chr3:45438405:C>T
LARS2
NM_015340:c.234+2226C>T
INTRON3
Unknown significance
rs559607579
This variant is a VUS because it does not have enough information.
553097
chr3:45438411:G>A
LARS2
NM_015340:c.234+2232G>A
INTRON3
Unknown significance
rs766061193
This variant is a VUS because it does not have enough information.
553098
chr3:45438421:T>G
LARS2
NM_015340:c.234+2242T>G
INTRON3
Unknown significance
rs756679217
This variant is a VUS because it does not have enough information.
553099
chr3:45438473:C>T
LARS2
NM_015340:c.234+2294C>T
INTRON3
Unknown significance
rs778167352
This variant is a VUS because it does not have enough information.
553100
chr3:45438474:G>A
LARS2
NM_015340:c.234+2295G>A
INTRON3
Unknown significance
rs62244087
This variant is a VUS because it does not have enough information.
553101
chr3:45438479:C>T
LARS2
NM_015340:c.234+2300C>T
INTRON3
Benign
rs545231501
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
553102
chr3:45438480:C>A
LARS2
NM_015340:c.234+2301C>A
INTRON3
Unknown significance
rs559306615
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
553103
chr3:45438498:T>C
LARS2
NM_015340:c.234+2319T>C
INTRON3
Unknown significance
rs771358133
This variant is a VUS because it does not have enough information.
553104
chr3:45438537:G>A
LARS2
NM_015340:c.234+2358G>A
INTRON3
Benign
rs142749511
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
0
1322
0
13
1006
0.0129
6
694
0.0086
0
1008
0
0
978
0
19
5008
0.00379393
</