762745
chr7:45613857:G>A
ADCY1
Unknown significance
rs369786422
This variant is a VUS because it does not have enough information.
762746
chr7:45613955:C>G
ADCY1
Unknown significance
rs561544199
This variant is a VUS because it does not have enough information.
0
1322
0
4
1006
0.004
2
694
0.0029
0
1008
0
0
978
0
6
5008
0.00119808
762747
chr7:45614145:G>-
ADCY1
NM_021116:c.3delG
EXON1
Unknown significance
rs567962651
4
1322
0.003
0
1006
0
0
694
0
1
1008
0.001
6
978
0.0061
11
5008
0.00219649
762748
chr7:45614242:C>G
ADCY1
NM_021116:p.Arg34Gly
NM_021116:c.100C>G
EXON1
Benign
rs760606743
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
0.691
N
0.389
T
0.0
B
0.188742
U
1
N;N
-0.384
N
1
4
0.25
0
0
0
0
12
0
0
0
0
0
28
0
0
4
0
0
156
0
1
204
0.00490196
762749
chr7:45614280:G>A
ADCY1
NM_021116:p.Glu46Glu
NM_021116:c.138G>A
EXON1
Unknown significance
rs764099850
This variant is a VUS because it does not have enough information.
0
32
0
0
22
0
0
50
0
0
0
0
1
402
0.00248756
0
26
0
0
1416
0
1
1948
0.000513347
762750
chr7:45614307:G>A
ADCY1
NM_021116:p.Arg55Arg
NM_021116:c.165G>A
EXON1
Unknown significance
rs753933695
This variant is a VUS because it does not have enough information.
0
56
0
0
28
0
0
60
0
0
2
0
1
534
0.00187266
0
34
0
0
2008
0
1
2722
0.000367377
762751
chr7:45614312:A>G
ADCY1
NM_021116:p.Glu57Gly
NM_021116:c.170A>G
EXON1
Unknown significance
rs552168629
This variant is a VUS because it does not have enough information.
0.092
N
0.059
T
0.996
D
0
D
0.999454
D;D
2.81
C
762752
chr7:45614346:C>T
ADCY1
NM_021116:p.Leu68Leu
NM_021116:c.204C>T
EXON1
Unknown significance
rs531991756
This variant is a VUS because it does not have enough information.
0
1322
0
2
1006
0.002
1
694
0.0014
0
1008
0
0
978
0
3
5008
0.000599042
762753
chr7:45614359:G>A
ADCY1
NM_021116:p.Gly73Ser
NM_021116:c.217G>A
EXON1
Likely benign
rs544024276
Pathogenicity is based on prediction data only. 2 out of 6 predictions were pathogenic.
0.875
N
0.494
T
0.003
B
0.028641
N
0.987602
D;D
3.96
C
0
1322
0
1
1006
0.001
0
694
0
0
1008
0
0
978
0
1
5008
0.000199681
762755
chr7:45614376:C>A
ADCY1
NM_021116:p.Ala78Ala
NM_021116:c.234C>A
EXON1
Benign
rs74641956
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
0
276
0
0
108
0
4
256
0.015625
0
366
0
0
2540
0
0
84
0
0
4932
0
4
8562
0.000467181
762754
chr7:45614376:C>G
ADCY1
NM_021116:p.Ala78Ala
NM_021116:c.234C>G
EXON1
Benign
rs74641956
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
6
694
0.0086
0
1008
0
0
978
0
25
5008
0.00499201
4
276
0.0144928
4
108
0.037037
0
256
0
20
366
0.0546448
240
2540
0.0944882
1
84
0.0119048
19
4932
0.00385239
288
8562
0.033637
762756
chr7:45614388:C>A
ADCY1
NM_021116:p.Gly82Gly
NM_021116:c.246C>A
EXON1
Unknown significance
rs758855790
This variant is a VUS because it does not have enough information.
1
930
0.00107527
0
578
0
0
978
0
0
550
0
0
6586
0
0
166
0
0
7046
0
1
16834
0.0000594036
762757
chr7:45614390:C>T
ADCY1
NM_021116:p.Ala83Val
NM_021116:c.248C>T
EXON1
Benign
rs375141353
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
0.783
N
0.317
T
0.715
P
0.324801
N
1
D;N
0.505
C
0
1322
0
0
1006
0
0
694
0
0
1008
0
8
978
0.0082
8
5008
0.00159744
0
1134
0
1
754
0.00132626
0
1228
0
0
820
0
0
8144
0
1
190
0.00526316
115
7668
0.0149974
117
19938
0.00586819
762758
chr7:45614391:G>T
ADCY1
NM_021116:p.Ala83Ala
NM_021116:c.249G>T
EXON1
Unknown significance
rs747493330
This variant is a VUS because it does not have enough information.
0
1340
0
0
932
0
1
1424
0.000702247
0
1012
0
0
9664
0
0
200
0
0
8134
0
1
22706
0.0000440412
762759
chr7:45614392:C>T
ADCY1
NM_021116:p.Pro84Ser
NM_021116:c.250C>T
EXON1
Unknown significance
rs79229229
This variant is a VUS because it does not have enough information.
0.783
N
0.436
T
0.759
P
0.000011
D
0.852915
D;D
3.69
C
762760
chr7:45614400:C>G
ADCY1
NM_021116:p.Pro86Pro
NM_021116:c.258C>G
EXON1
Benign
rs200597993
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
1
1322
0.0008
1
1006
0.001
2
694
0.0029
0
1008
0
1
978
0.001
5
5008
0.000998403
2
2838
0.000704722
1
3068
0.000325945
0
3356
0
0
1930
0
40
22654
0.00176569
0
336
0
105
10216
0.010278
148
44398
0.00333348
762761
chr7:45614400:C>T
ADCY1
NM_021116:p.Pro86Pro
NM_021116:c.258C>T
EXON1
Unknown significance
rs200597993
This variant is a VUS because it does not have enough information.
0
2838
0
0
3068
0
0
3356
0
0
1930
0
1
22654
0.0000441423
1
336
0.00297619
0
10216
0
2
44398
0.0000450471
762762
chr7:45614401:G>C
ADCY1
NM_021116:p.Ala87Pro
NM_021116:c.259G>C
EXON1
Unknown significance
rs748845827
This variant is a VUS because it does not have enough information.
0.874
N
0.142
T
0.574
P
0.00026
D
0.703355
D;D
2.8
C
0
2956
0
0
3310
0
0
3524
0
0
1956
0
1
24142
0.0000414216
0
346
0
0
10406
0
1
46640
0.0000214408
762763
chr7:45614405:C>T
ADCY1
NM_021116:p.Pro88Leu
NM_021116:c.263C>T
EXON1
Likely benign
rs770682134
Pathogenicity is based on prediction data only. 2 out of 6 predictions were pathogenic.
-0.068
N
0.662
T
0.0
B
0.007712
N
0.986981
D;D
2.8
C
0
3980
0
2
5362
0.000372995
0
4798
0
0
2816
0
0
33858
0
0
452
0
0
11588
0
2
62854
0.0000318198
762764
chr7:45614407:G>A
ADCY1
NM_021116:p.Gly89Ser
NM_021116:c.265G>A
EXON1
Unknown significance
rs79204521
This variant is a VUS because it does not have enough information.
0.874
N
0.424
T
0.014
B
0.000142
D
1
D;N
2.69
C
762765
chr7:45614410:C>G
ADCY1
NM_021116:p.Leu90Val
NM_021116:c.268C>G
EXON1
Unknown significance
rs774107345
This variant is a VUS because it does not have enough information.
0.792
N
0.25
T
0.006
B
0.000117
D
1
D;N
3.69
C
0
5234
0
0
7780
0
0
6164
0
0
3810
0
1
44284
0.0000225815
0
570
0
0
12858
0
1
80700
0.0000123916
762766
chr7:45614414:C>T
ADCY1
NM_021116:p.Ala91Val
NM_021116:c.272C>T
EXON1
Unknown significance
rs77566296
This variant is a VUS because it does not have enough information.
0.792
N
0.64
T
0.501
P
0.00001
D
0.962163
D;D
2.8
C
762767
chr7:45614417:A>G
ADCY1
NM_021116:p.Lys92Arg
NM_021116:c.275A>G
EXON1
Likely benign
rs745641221
Pathogenicity is based on prediction data only. 2 out of 6 predictions were pathogenic.
0.097
N
0.486
T
0.002
B
0.000008
N
0.998817
D;D
2.53
C
0
6360
0
0
9694
0
0
7348
0
0
4790
0
0
52796
0
1
684
0.00146199
0
14118
0
1
95790
0.0000104395
762768
chr7:45614419:G>T
ADCY1
NM_021116:p.Gly93Cys
NM_021116:c.277G>T
EXON1
Unknown significance
rs771838265
This variant is a VUS because it does not have enough information.
0.884
N
0.163
T
1.0
D
0
D
0.999989
D;D
3.69
C
0
6546
0
0
9984
0
0
7514
0
0
4952
0
1
54064
0.0000184966
0
700
0
0
14356
0
1
98116
0.000010192
762769
chr7:45614430:G>A
ADCY1
NM_021116:p.Pro96Pro
NM_021116:c.288G>A
EXON1
Unknown significance
rs775165471
This variant is a VUS because it does not have enough information.
0
7452
0
0
10840
0
0
8102
0
0
5688
0
1
58884
0.0000169825
0
776
0
0
15454
0
1
107196
0.00000932871
762770
chr7:45614439:C>T
ADCY1
NM_021116:p.Cys99Cys
NM_021116:c.297C>T
EXON1
Unknown significance
rs776113547
This variant is a VUS because it does not have enough information.
0
7900
0
0
11036
0
0
8236
0
0
6046
0
1
60458
0.0000165404
0
792
0
0
15888
0
1
110356
0.00000906158
762771
chr7:45614440:G>A
ADCY1
NM_021116:p.Val100Ile
NM_021116:c.298G>A
EXON1
Likely benign
rs764052766
Pathogenicity is based on prediction data only. 2 out of 6 predictions were pathogenic.
0.045
N
0.83
T
0.003
B
0.002557
N
1
D;N
1.58
C
0
7950
0
0
11056
0
0
8248
0
0
6086
0
0
60648
0
0
798
0
1
15930
0.0000627746
1
110716
0.00000903212
762772
chr7:45614440:G>C
ADCY1
NM_021116:p.Val100Leu
NM_021116:c.298G>C
EXON1
Likely benign
rs764052766
Pathogenicity is based on prediction data only. 2 out of 6 predictions were pathogenic.
0.045
N
0.47
T
0.079
B
0.002557
N
1
D;N
1.58
C
0
7950
0
0
11056
0
0
8248
0
0
6086
0
1
60648
0.0000164886
0
798
0
0
15930
0
1
110716
0.00000903212
762773
chr7:45614442:C>T
ADCY1
NM_021116:p.Val100Val
NM_021116:c.300C>T
EXON1
Unknown significance
rs761931194
This variant is a VUS because it does not have enough information.
0
8038
0
0
11084
0
0
8266
0
0
6142
0
1
60856
0.0000164322
0
804
0
1
15974
0.0000626017
2
111164
0.0000179914
762774
chr7:45614454:G>A
ADCY1
NM_021116:p.Ala104Ala
NM_021116:c.312G>A
EXON1
Unknown significance
rs765365053
This variant is a VUS because it does not have enough information.
0
8236
0
0
11182
0
0
8306
0
0
6318
0
1
61504
0.0000162591
0
824
0
0
16170
0
1
112540
0.00000888573
762775
chr7:45614461:G>C
ADCY1
NM_021116:p.Val107Leu
NM_021116:c.319G>C
EXON1
Unknown significance
rs200378809
This variant is a VUS because it does not have enough information.
0.884
N
0.08
T
0.002
B
0.000055
D
0.988785
D;D
2.47
C
0
8322
0
0
11214
0
0
8316
0
1
6394
0.000156397
0
61686
0
0
836
0
0
16226
0
1
112994
0.00000885003
762776
chr7:45614461:G>T
ADCY1
NM_021116:p.Val107Leu
NM_021116:c.319G>T
EXON1
Unknown significance
rs200378809
This variant is a VUS because it does not have enough information.
0.884
N
0.08
T
0.002
B
0.000055
D
0.989214
D;D
2.47
C
0
8322
0
0
11214
0
2
8316
0.0002405
0
6394
0
0
61686
0
0
836
0
0
16226
0
2
112994
0.0000177001
762777
chr7:45614472:CGT>-
ADCY1
NM_021116:c.330_332delCGT
EXON1
Unknown significance
rs761370974
This variant is a VUS because it does not have enough information.
762778
chr7:45614482:C>T
ADCY1
NM_021116:p.Leu114Leu
NM_021116:c.340C>T
EXON1
Unknown significance
rs766716634
This variant is a VUS because it does not have enough information.
0
8392
0
0
11258
0
0
8346
0
0
6450
0
0
61860
0
0
832
0
1
16280
0.0000614251
1
113418
0.00000881694
762779
chr7:45614499:G>A
ADCY1
NM_021116:p.Leu119Leu
NM_021116:c.357G>A
EXON1
Unknown significance
rs752002367
This variant is a VUS because it does not have enough information.
0
8442
0
0
11272
0
0
8342
0
0
6456
0
1
61946
0.0000161431
0
838
0
0
16274
0
1
113570
0.00000880514
762780
chr7:45614508:C>T
ADCY1
NM_021116:p.Val122Val
NM_021116:c.366C>T
EXON1
Unknown significance
rs755508070
This variant is a VUS because it does not have enough information.
0
8486
0
0
11268
0
0
8332
0
0
6442
0
0
61962
0
0
842
0
1
16274
0.0000614477
1
113606
0.00000880235
762781
chr7:45614533:C>T
ADCY1
NM_021116:p.Leu131Phe
NM_021116:c.391C>T
EXON1
Unknown significance
rs781776242
This variant is a VUS because it does not have enough information.
0.792
N
0.3
T
0.0
B
0.000013
D
0.886263
D;D
2.55
C
0
8490
0
0
11234
0
0
8328
0
0
6416
0
0
61802
0
0
842
0
1
16240
0.0000615764
1
113352
0.00000882208
762782
chr7:45614535:C>G
ADCY1
NM_021116:p.Leu131Leu
NM_021116:c.393C>G
EXON1
Unknown significance
rs753381717
This variant is a VUS because it does not have enough information.
0
8480
0
0
11234
0
0
8328
0
0
6412
0
0
61774
0
0
842
0
2
16232
0.000123213
2
113302
0.0000176519
762783
chr7:45614544:G>T
ADCY1
NM_021116:p.Ala134Ala
NM_021116:c.402G>T
EXON1
Unknown significance
rs756854830
This variant is a VUS because it does not have enough information.
0
8356
0
0
11202
0
0
8290
0
0
6364
0
0
61458
0
0
836
0
1
16196
0.0000617436
1
112702
0.00000887296
762784
chr7:45614550:C>T
ADCY1
NM_021116:p.Leu136Leu
NM_021116:c.408C>T
EXON1
Unknown significance
rs778295490
This variant is a VUS because it does not have enough information.
0
8332
0
1
11178
0.0000894614
0
8272
0
0
6366
0
0
61312
0
0
834
0
0
16182
0
1
112476
0.00000889079
762785
chr7:45614551:->CCCTTACA
ADCY1
NM_021116:c.409_410insCCCTTACA
EXON1
Unknown significance
rs767679562
This variant is a VUS because it does not have enough information.
0
8332
0
0
11178
0
0
8272
0
0
6366
0
1
61312
0.00001631
0
834
0
0
16182
0
1
112476
0.00000889079
762786
chr7:45614553:->TAATCATCCAAATGGGAGTGGGTGGT
ADCY1
NM_021116:c.411_412insTAATCATCCAAATGGGAGTGGGTGGT
EXON1
Unknown significance
rs750467665
This variant is a VUS because it does not have enough information.
762787
chr7:45614555:->A
ADCY1
NM_021116:c.413_414insA
EXON1
Unknown significance
rs761016108
This variant is a VUS because it does not have enough information.
0
8242
0
0
11146
0
0
8250
0
0
6340
0
1
60870
0.0000164285
0
830
0
0
16162
0
1
111840
0.00000894134
762788
chr7:45614556:T>C
ADCY1
NM_021116:p.Cys138Cys
NM_021116:c.414T>C
EXON1
Unknown significance
rs745471312
This variant is a VUS because it does not have enough information.
0
8208
0
0
11128
0
0
8240
0
0
6334
0
1
60674
0.0000164815
0
828
0
0
16148
0
1
111560
0.00000896379
762789
chr7:45614562:C>G
ADCY1
NM_021116:p.Phe140Leu
NM_021116:c.420C>G
EXON1
Likely benign
rs771648046
Pathogenicity is based on prediction data only. 1 out of 6 predictions were pathogenic.
-0.061
N
1.0
T
0.006
B
0.000006
N
0.983344
D;D
-4.67
N
1
8008
0.000124875
0
11078
0
0
8142
0
0
6304
0
0
59560
0
0
812
0
0
16112
0
1
110016
0.00000908959
762790
chr7:45614563:G>T
ADCY1
NM_021116:p.Ala141Ser
NM_021116:c.421G>T
EXON1
Unknown significance
rs779862034
This variant is a VUS because it does not have enough information.
0.884
N
0.524
T
0.014
B
0.000041
D
1
D;N
1.46
C
0
7962
0
0
11082
0
0
8130
0
0
6292
0
1
59334
0.0000168537
0
812
0
0
16094
0
1
109706
0.00000911527
762791
chr7:45614565:G>C
ADCY1
NM_021116:p.Ala141Ala
NM_021116:c.423G>C
EXON1
Unknown significance
rs746848171
This variant is a VUS because it does not have enough information.
0
7972
0
0
11066
0
0
8130
0
0
6294
0
6
59344
0.000101105
0
812
0
3
16106
0.000186266
9
109724
0.000082024
762792
chr7:45614565:G>T
ADCY1
NM_021116:p.Ala141Ala
NM_021116:c.423G>T
EXON1
Unknown significance
rs746848171
This variant is a VUS because it does not have enough information.
0
7972
0
0
11066
0
0
8130
0
0
6294
0
1
59344
0.0000168509
0
812
0
0
16106
0
1
109724
0.00000911378
762793
chr7:45614571:C>G
ADCY1
NM_021116:p.Gly143Gly
NM_021116:c.429C>G
EXON1
Unknown significance
rs764921404
This variant is a VUS because it does not have enough information.
762794
chr7:45614576:C>T
ADCY1
NM_021116:p.Pro145Leu
NM_021116:c.434C>T
EXON1
Unknown significance
rs776609542
This variant is a VUS because it does not have enough information.
0.792
N
0.026
D
0.137
B
0.00339
N
0.997957
D;D
2.84
C
0
7702
0
0
10956
0
0
8018
0
0
6240
0
2
57924
0.000034528
0
794
0
0
16058
0
2
107692
0.0000185715
762795
chr7:45614582:G>A
ADCY1
NM_021116:p.Arg147Gln
NM_021116:c.440G>A
EXON1
Likely benign
rs761877943
Pathogenicity is based on prediction data only. 2 out of 5 predictions were pathogenic.
0.884
N
0.593
T
0.178
B
0.92601
U
0.99998
D;N
2.84
C
0
7624
0
0
10932
0
0
7988
0
0
6218
0
0
57626
0
0
794
0
1
16060
0.0000622665
1
107242
0.0000093247
762796
chr7:45614582:G>C
ADCY1
NM_021116:p.Arg147Pro
NM_021116:c.440G>C
EXON1
Likely benign
rs761877943
Pathogenicity is based on prediction data only. 2 out of 5 predictions were pathogenic.
0.884
N
0.309
T
0.165
B
0.92601
U
0.999984
D;N
2.84
C
0
7624
0
0
10932
0
1
7988
0.000125188
0
6218
0
0
57626
0
0
794
0
0
16060
0
1
107242
0.0000093247
762797
chr7:45614595:G>C
ADCY1
NM_021116:p.Gly151Gly
NM_021116:c.453G>C
EXON1
Unknown significance
rs773187376
This variant is a VUS because it does not have enough information.
0
7590
0
0
10888
0
0
7928
0
0
6162
0
0
57274
0
0
784
0
1
16056
0.000062282
1
106682
0.00000937365
762798
chr7:45614603:G>T
ADCY1
NM_021116:p.Gly154Val
NM_021116:c.461G>T
EXON1
Likely benign
rs763194212
Pathogenicity is based on prediction data only. 0 out of 6 predictions were pathogenic.
-0.976
N
0.354
T
0.0
B
0.169948
N
0.999999
N;N
-0.53
N
0
7632
0
0
10866
0
2
7930
0.000252207
0
6168
0
0
57376
0
0
780
0
0
16048
0
2
106800
0.0000187266
762799
chr7:45614604:G>A
ADCY1
NM_021116:p.Gly154Gly
NM_021116:c.462G>A
EXON1
Unknown significance
rs766548504
This variant is a VUS because it does not have enough information.
0
7702
0
0
10898
0
0
7956
0
0
6178
0
3
57516
0.0000521594
0
790
0
0
16066
0
3
107106
0.0000280096
762800
chr7:45614605:G>A
ADCY1
NM_021116:p.Gly155Arg
NM_021116:c.463G>A
EXON1
Likely benign
rs751947495
Pathogenicity is based on prediction data only. 1 out of 6 predictions were pathogenic.
0.884
N
0.543
T
0.0
B
0.001985
N
0.999974
N;N
2.7
C
0
7704
0
0
10900
0
0
7948
0
0
6162
0
1
57510
0.0000173883
0
790
0
0
16070
0
1
107084
0.00000933846
762801
chr7:45614636:A>C
ADCY1
NM_021116:p.Gln165Pro
NM_021116:c.494A>C
EXON1
Unknown significance
rs760033357
This variant is a VUS because it does not have enough information.
1.011
C
0.266
T
0.002
B
0
D
0.999975
D;D
3.7
C
0
8412
0
0
11024
0
0
8156
0
0
6242
0
1
59438
0.0000168243
0
812
0
0
16144
0
1
110228
0.00000907211
762802
chr7:45614643:T>G
ADCY1
NM_021116:p.Leu167Leu
NM_021116:c.501T>G
EXON1
Unknown significance
rs376573772
This variant is a VUS because it does not have enough information.
1
8548
0.000116986
0
4382
0
1
12930
0.0000773395
762803
chr7:45614652:C>T
ADCY1
NM_021116:p.Thr170Thr
NM_021116:c.510C>T
EXON1
Unknown significance
rs370830411
This variant is a VUS because it does not have enough information.
0
8556
0
1
4390
0.00022779
1
12946
0.0000772439
1
8642
0.000115714
0
11092
0
0
8272
0
0
6268
0
0
60340
0
0
818
0
0
16166
0
1
111598
0.00000896073
762804
chr7:45614663:A>G
ADCY1
NM_021116:p.Tyr174Cys
NM_021116:c.521A>G
EXON1
Unknown significance
rs753183956
This variant is a VUS because it does not have enough information.
1.011
C
0.001
D
0.999
D
0.000002
D
0.999999
D;D
3.7
C
0
8758
0
0
11146
0
0
8326
0
0
6284
0
0
60848
0
0
820
0
1
16192
0.0000617589
1
112374
0.00000889886
762805
chr7:45614671:C>A
ADCY1
NM_021116:p.Leu177Met
NM_021116:c.529C>A
EXON1
Unknown significance
rs756596808
This variant is a VUS because it does not have enough information.
0.797
N
0.293
T
0.996
D
0.000021
D
0.999722
D;D
3.7
C
0
8794
0
0
11154
0
0
8342
0
0
6298
0
1
61004
0.0000163924
0
820
0
0
16196
0
1
112608
0.00000888036
762806
chr7:45614685:C>A
ADCY1
NM_021116:p.Ser181Arg
NM_021116:c.543C>A
EXON1
Unknown significance
rs778441100
This variant is a VUS because it does not have enough information.
0.797
N
0.022
D
0.009
B
0.000006
D
1
D;N
2.56
C
0
8866
0
0
11210
0
1
8384
0.000119275
0
6282
0
0
61292
0
0
820
0
0
16186
0
1
113040
0.00000884643
762807
chr7:45614685:C>G
ADCY1
NM_021116:p.Ser181Arg
NM_021116:c.543C>G
EXON1
Unknown significance
rs778441100
This variant is a VUS because it does not have enough information.
0.797
N
0.022
D
0.009
B
0.000006
D
1
D;N
2.56
C
0
8866
0
0
11210
0
0
8384
0
0
6282
0
0
61292
0
0
820
0
2
16186
0.000123564
2
113040
0.0000176929
762808
chr7:45614693:C>T
ADCY1
NM_021116:p.Ala184Val
NM_021116:c.551C>T
EXON1
Unknown significance
rs758041210
This variant is a VUS because it does not have enough information.
-0.019
N
0.002
D
0.907
P
0.000251
N
0.999979
D;D
1.88
C
0
8900
0
0
11228
0
0
8398
0
0
6296
0
1
61416
0.0000162824
0
830
0
0
16162
0
1
113230
0.00000883158
762809
chr7:45614697:A>G
ADCY1
NM_021116:p.Ile185Met
NM_021116:c.555A>G
EXON1
Unknown significance
rs779732430
This variant is a VUS because it does not have enough information.
-0.022
N
0.006
D
0.311
B
0.000032
D
0.995697
D;D
3.7
C
0
8914
0
0
11220
0
0
8400
0
0
6302
0
1
61478
0.000016266
0
828
0
0
16154
0
1
113296
0.00000882644
762810
chr7:45614707:C>T
ADCY1
NM_021116:p.Leu189Phe
NM_021116:c.565C>T
EXON1
Likely benign
rs765505992
Pathogenicity is based on prediction data only. 2 out of 6 predictions were pathogenic.
0.797
N
0.259
T
0.011
B
0.049104
N
0.898464
D;D
2.71
C
0
8794
0
0
11216
0
0
8400
0
0
6270
0
1
61338
0.0000163031
0
826
0
0
16088
0
1
112932
0.00000885489
762811
chr7:45614709:C>T
ADCY1
NM_021116:p.Leu189Leu
NM_021116:c.567C>T
EXON1
Unknown significance
rs768506366
This variant is a VUS because it does not have enough information.
1
8816
0.00011343
0
11222
0
0
8394
0
0
6270
0
0
61364
0
0
824
0
0
16092
0
1
112982
0.00000885097
762812
chr7:45614742:C>T
ADCY1
NM_021116:p.Ala200Ala
NM_021116:c.600C>T
EXON1
Unknown significance
rs780969675
This variant is a VUS because it does not have enough information.
0
8754
0
1
11280
0.0000886525
0
8436
0
0
6288
0
0
61204
0
0
818
0
0
15284
0
1
112064
0.00000892347
762813
chr7:45614744:C>T
ADCY1
NM_021116:p.Thr201Ile
NM_021116:c.602C>T
EXON1
Unknown significance
rs748029352
This variant is a VUS because it does not have enough information.
0.864
N
0.398
T
0.001
B
0.000189
D
0.970849
D;D
3.7
C
0
8726
0
0
11274
0
0
8442
0
0
6290
0
1
61188
0.0000163431
0
816
0
0
15180
0
1
111916
0.00000893527
762814
chr7:45614757:C>T
ADCY1
NM_021116:p.Ala205Ala
NM_021116:c.615C>T
EXON1
Unknown significance
rs139122316
This variant is a VUS because it does not have enough information.
1
8568
0.000116713
0
4386
0
1
12954
0.0000771962
762815
chr7:45614796:G>A
ADCY1
NM_021116:c.639+15G>A
INTRON1
Unknown significance
rs769649414
This variant is a VUS because it does not have enough information.
0
8342
0
2
11184
0.000178827
0
8390
0
0
6216
0
0
59842
0
0
738
0
0
11354
0
2
106066
0.0000188562
762816
chr7:45614798:A>T
ADCY1
NM_021116:c.639+17A>T
INTRON1
Unknown significance
rs773309750
This variant is a VUS because it does not have enough information.
0
8308
0
0
11188
0
0
8382
0
0
6200
0
10
59778
0.000167286
0
734
0
0
11196
0
10
105786
0.0000945305
762817
chr7:45614807:C>G
ADCY1
NM_021116:c.639+26C>G
INTRON1
Unknown significance
rs199544733
This variant is a VUS because it does not have enough information.
0
8504
0
5
4360
0.00114679
5
12864
0.000388682
1
1322
0.0008
0
1006
0
0
694
0
0
1008
0
0
978
0
1
5008
0.000199681
19
8238
0.00230639
3
11174
0.00026848
0
8356
0
0
6202
0
0
59428
0
0
722
0
0
10448
0
22
104568
0.000210389
762818
chr7:45614814:C>G
ADCY1
NM_021116:c.639+33C>G
INTRON1
Unknown significance
rs771168252
This variant is a VUS because it does not have enough information.
1
8184
0.00012219
0
11154
0
0
8346
0
0
6180
0
0
59210
0
0
716
0
0
9976
0
1
103766
0.00000963707
762819
chr7:45614817:A>G
ADCY1
NM_021116:c.639+36A>G
INTRON1
Unknown significance
rs774777802
This variant is a VUS because it does not have enough information.
0
8148
0
0
11152
0
0
8338
0
0
6172
0
1
59176
0.0000168987
0
710
0
0
9772
0
1
103468
0.00000966482
762820
chr7:45614822:C>T
ADCY1
NM_021116:c.639+41C>T
INTRON1
Unknown significance
rs759838946
This variant is a VUS because it does not have enough information.
0
8048
0
0
11128
0
0
8322
0
0
6126
0
0
58940
0
0
706
0
1
9422
0.000106135
1
102692
0.00000973786
762821
chr7:45614823:T>C
ADCY1
NM_021116:c.639+42T>C
INTRON1
Unknown significance
rs767939227
This variant is a VUS because it does not have enough information.
1
8056
0.000124131
0
11122
0
0
8318
0
0
6142
0
0
58958
0
0
708
0
0
9446
0
1
102750
0.00000973236
762822
chr7:45614825:G>A
ADCY1
NM_021116:c.639+44G>A
INTRON1
Unknown significance
rs776023135
This variant is a VUS because it does not have enough information.
0
8010
0
0
11122
0
0
8308
0
0
6134
0
2
58882
0.0000339662
0
708
0
0
9406
0
2
102570
0.0000194989
762823
chr7:45614826:C>G
ADCY1
NM_021116:c.639+45C>G
INTRON1
Unknown significance
rs761208011
This variant is a VUS because it does not have enough information.
0
7996
0
0
11118
0
0
8300
0
1
6114
0.000163559
0
58784
0
0
700
0
0
9298
0
1
102310
0.00000977422
762824
chr7:45614828:G>A
ADCY1
NM_021116:c.639+47G>A
INTRON1
Unknown significance
rs764551512
This variant is a VUS because it does not have enough information.
762825
chr7:45614848:C>G
ADCY1
NM_021116:c.639+67C>G
INTRON1
Unknown significance
rs529625280
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
762826
chr7:45614859:G>A
ADCY1
NM_021116:c.639+78G>A
INTRON1
Unknown significance
rs548105209
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
762827
chr7:45614874:C>T
ADCY1
NM_021116:c.639+93C>T
INTRON1
Unknown significance
rs569611079
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
762828
chr7:45614875:G>A
ADCY1
NM_021116:c.639+94G>A
INTRON1
Benign
rs73318930
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
29
1322
0.0219
38
1006
0.0378
22
694
0.0317
0
1008
0
10
978
0.0102
99
5008
0.0197684
762829
chr7:45614906:G>A
ADCY1
NM_021116:c.639+125G>A
INTRON1
Unknown significance
rs568560081
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
762830
chr7:45614925:C>G
ADCY1
NM_021116:c.639+144C>G
INTRON1
Unknown significance
rs570597916
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
762831
chr7:45614927:A>G
ADCY1
NM_021116:c.639+146A>G
INTRON1
Unknown significance
rs538774158
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
762832
chr7:45614958:C>G
ADCY1
NM_021116:c.639+177C>G
INTRON1
Unknown significance
rs554225387
This variant is a VUS because it does not have enough information.
1
1322
0.0008
0
1006
0
0
694
0
0
1008
0
1
978
0.001
2
5008
0.000399361
762833
chr7:45614985:C>A
ADCY1
NM_021116:c.639+204C>A
INTRON1
Unknown significance
rs528174506
This variant is a VUS because it does not have enough information.
762834
chr7:45615035:G>A
ADCY1
NM_021116:c.639+254G>A
INTRON1
Unknown significance
rs572378362
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
762835
chr7:45615063:G>C
ADCY1
NM_021116:c.639+282G>C
INTRON1
Unknown significance
rs763312122
This variant is a VUS because it does not have enough information.
762836
chr7:45615114:C>T
ADCY1
NM_021116:c.639+333C>T
INTRON1
Unknown significance
rs543041940
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
762837
chr7:45615137:T>G
ADCY1
NM_021116:c.639+356T>G
INTRON1
Unknown significance
rs764326617
This variant is a VUS because it does not have enough information.
762838
chr7:45615164:C>G
ADCY1
NM_021116:c.639+383C>G
INTRON1
Unknown significance
rs752132116
This variant is a VUS because it does not have enough information.
762839
chr7:45615175:C>T
ADCY1
NM_021116:c.639+394C>T
INTRON1
Unknown significance
rs555345101
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
762840
chr7:45615183:G>A
ADCY1
NM_021116:c.639+402G>A
INTRON1
Benign
rs373380741
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
762841
chr7:45615185:C>G
ADCY1
NM_021116:c.639+404C>G
INTRON1
Benign
rs12702148
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
81
1322
0.0613
313
1006
0.3111
199
694
0.2867
474
1008
0.4702
345
978
0.3528
1412
5008
0.281949
762842
chr7:45615193:G>A
ADCY1
NM_021116:c.639+412G>A
INTRON1
Unknown significance
rs375745430
This variant is a VUS because it does not have enough information.
762843
chr7:45615209:C>A
ADCY1
NM_021116:c.639+428C>A
INTRON1
Unknown significance
rs565357511
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
762844
chr7:45615249:C>T
ADCY1
NM_021116:c.639+468C>T
INTRON1
Unknown significance
rs184559465
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
762845
chr7:45615260:C>T
ADCY1
NM_021116:c.639+479C>T
INTRON1
Benign
rs145162581
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
0
1322
0
12
1006
0.0119
2
694
0.0029
0
1008
0
6
978
0.0061
20
5008
0.00399361
762846
chr7:45615264:G>T
ADCY1
NM_021116:c.639+483G>T
INTRON1
Unknown significance
rs751487247
This variant is a VUS because it does not have enough information.
762847
chr7:45615289:A>T
ADCY1
NM_021116:c.639+508A>T
INTRON1
Unknown significance
rs559375449
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
762848
chr7:45615303:A>C
ADCY1
NM_021116:c.639+522A>C
INTRON1
Unknown significance
rs369011235
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
762849
chr7:45615333:C>T
ADCY1
NM_021116:c.639+552C>T
INTRON1
Unknown significance
rs749959431
This variant is a VUS because it does not have enough information.
762850
chr7:45615382:C>T
ADCY1
NM_021116:c.639+601C>T
INTRON1
Benign
rs189331207
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
14
1322
0.0106
0
1006
0
0
694
0
0
1008
0
0
978
0
14
5008
0.00279553
762851
chr7:45615385:T>A
ADCY1
NM_021116:c.639+604T>A
INTRON1
Unknown significance
rs755627358
This variant is a VUS because it does not have enough information.
762852
chr7:45615399:G>C
ADCY1
NM_021116:c.639+618G>C
INTRON1
Unknown significance
rs779853539
This variant is a VUS because it does not have enough information.
762853
chr7:45615402:G>-
ADCY1
NM_021116:c.639+621delG
INTRON1
Unknown significance
rs534965150
This variant is a VUS because it does not have enough information.
1
1322
0.0008
0
1006
0
0
694
0
2
1008
0.002
0
978
0
3
5008
0.000599042
762854
chr7:45615460:C>T
ADCY1
NM_021116:c.639+679C>T
INTRON1
Unknown significance
rs562902921
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
762855
chr7:45615478:G>C
ADCY1
NM_021116:c.639+697G>C
INTRON1
Unknown significance
rs369341105
This variant is a VUS because it does not have enough information.
762856
chr7:45615481:C>T
ADCY1
NM_021116:c.639+700C>T
INTRON1
Unknown significance
rs370121629
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
762857
chr7:45615482:G>A
ADCY1
NM_021116:c.639+701G>A
INTRON1
Unknown significance
rs552414012
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
762858
chr7:45615605:T>C
ADCY1
NM_021116:c.639+824T>C
INTRON1
Benign
rs181985809
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
4
1322
0.003
28
1006
0.0278
5
694
0.0072
10
1008
0.0099
101
978
0.1033
148
5008
0.0295527
762859
chr7:45615617:C>T
ADCY1
NM_021116:c.639+836C>T
INTRON1
Unknown significance
rs556886268
This variant is a VUS because it does not have enough information.
762860
chr7:45615627:G>A
ADCY1
NM_021116:c.639+846G>A
INTRON1
Benign
rs7804852
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
32
1322
0.0242
0
1006
0
2
694
0.0029
0
1008
0
0
978
0
34
5008
0.00678914
762861
chr7:45615628:C>T
ADCY1
NM_021116:c.639+847C>T
INTRON1
Benign
rs7804581
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
32
1322
0.0242
0
1006
0
2
694
0.0029
0
1008
0
0
978
0
34
5008
0.00678914
762862
chr7:45615646:G>-
ADCY1
NM_021116:c.639+865delG
INTRON1
Unknown significance
rs200909534
This variant is a VUS because it does not have enough information.
762863
chr7:45615647:T>-
ADCY1
NM_021116:c.639+866delT
INTRON1
Benign
rs11339042
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
685
1322
0.5182
482
1006
0.4791
294
694
0.4236
673
1008
0.6677
603
978
0.6166
2737
5008
0.546526
762864
chr7:45615648:T>G
ADCY1
NM_021116:c.639+867T>G
INTRON1
Unknown significance
rs199943201
This variant is a VUS because it does not have enough information.
762865
chr7:45615676:G>A
ADCY1
NM_021116:c.639+895G>A
INTRON1
Unknown significance
rs113821653
This variant is a VUS because it does not have enough information.
762866
chr7:45615704:G>T
ADCY1
NM_021116:c.639+923G>T
INTRON1
Unknown significance
rs566171167
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
762867
chr7:45615707:G>T
ADCY1
NM_021116:c.639+926G>T
INTRON1
Unknown significance
rs754839666
This variant is a VUS because it does not have enough information.
762868
chr7:45615757:C>T
ADCY1
NM_021116:c.639+976C>T
INTRON1
Unknown significance
rs778618608
This variant is a VUS because it does not have enough information.
762869
chr7:45615765:A>G
ADCY1
NM_021116:c.639+984A>G
INTRON1
Unknown significance
rs539366781
This variant is a VUS because it does not have enough information.
762870
chr7:45615783:C>T
ADCY1
NM_021116:c.639+1002C>T
INTRON1
Benign
rs12702149
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
264
1322
0.1997
400
1006
0.3976
251
694
0.3617
662
1008
0.6567
494
978
0.5051
2071
5008
0.413538
762871
chr7:45615797:GG>-
ADCY1
NM_021116:c.639+1016_639+1017delGG
INTRON1
Unknown significance
rs758751673
This variant is a VUS because it does not have enough information.
762872
chr7:45615803:G>A
ADCY1
NM_021116:c.639+1022G>A
INTRON1
Unknown significance
rs555009719
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
762873
chr7:45615823:A>G
ADCY1
NM_021116:c.639+1042A>G
INTRON1
Unknown significance
rs576474066
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
762874
chr7:45615829:T>A
ADCY1
NM_021116:c.639+1048T>A
INTRON1
Unknown significance
rs537357782
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
762875
chr7:45615842:C>G
ADCY1
NM_021116:c.639+1061C>G
INTRON1
Unknown significance
rs565848865
This variant is a VUS because it does not have enough information.
762876
chr7:45615851:G>A
ADCY1
NM_021116:c.639+1070G>A
INTRON1
Unknown significance
rs771972761
This variant is a VUS because it does not have enough information.
762877
chr7:45615860:G>A
ADCY1
NM_021116:c.639+1079G>A
INTRON1
Unknown significance
rs777757323
This variant is a VUS because it does not have enough information.
762878
chr7:45615880:G>A
ADCY1
NM_021116:c.639+1099G>A
INTRON1
Benign
rs77239239
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
38
1322
0.0287
30
1006
0.0298
22
694
0.0317
162
1008
0.1607
104
978
0.1063
356
5008
0.0710863
762879
chr7:45615918:G>A
ADCY1
NM_021116:c.639+1137G>A
INTRON1
Unknown significance
rs756184009
This variant is a VUS because it does not have enough information.
762880
chr7:45615921:TG>-
ADCY1
NM_021116:c.639+1140_639+1141delTG
INTRON1
Unknown significance
rs556672185
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
762881
chr7:45615942:CAGT>-
ADCY1
NM_021116:c.639+1161_639+1164delCAGT
INTRON1
Benign
rs367978525
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
5
1322
0.0038
5
1006
0.005
0
694
0
7
1008
0.0069
47
978
0.0481
64
5008
0.0127796
762882
chr7:45615956:A>G
ADCY1
NM_021116:c.639+1175A>G
INTRON1
Benign
rs4724419
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
1320
1322
0.9985
993
1006
0.9871
688
694
0.9914
1008
1008
1
978
978
1
4987
5008
0.995807
762883
chr7:45615968:A>G
ADCY1
NM_021116:c.639+1187A>G
INTRON1
Unknown significance
rs541609251
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
762884
chr7:45615970:C>A
ADCY1
NM_021116:c.639+1189C>A
INTRON1
Unknown significance
rs757581582
This variant is a VUS because it does not have enough information.
762885
chr7:45615979:G>A
ADCY1
NM_021116:c.639+1198G>A
INTRON1
Unknown significance
rs374189075
This variant is a VUS because it does not have enough information.
762886
chr7:45616041:G>T
ADCY1
NM_021116:c.639+1260G>T
INTRON1
Unknown significance
rs779252024
This variant is a VUS because it does not have enough information.
762887
chr7:45616075:C>T
ADCY1
NM_021116:c.639+1294C>T
INTRON1
Benign
rs11979797
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
164
1322
0.1241
50
1006
0.0497
27
694
0.0389
0
1008
0
7
978
0.0072
248
5008
0.0495208
762888
chr7:45616107:A>G
ADCY1
NM_021116:c.639+1326A>G
INTRON1
Unknown significance
rs763115041
This variant is a VUS because it does not have enough information.
762889
chr7:45616113:G>A
ADCY1
NM_021116:c.639+1332G>A
INTRON1
Benign
rs78436178
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
2
1322
0.0015
9
1006
0.0089
79
694
0.1138
302
1008
0.2996
45
978
0.046
437
5008
0.0872604
762890
chr7:45616131:A>C
ADCY1
NM_021116:c.639+1350A>C
INTRON1
Benign
rs11972954
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
26
1322
0.0197
0
1006
0
0
694
0
0
1008
0
0
978
0
26
5008
0.00519169
762891
chr7:45616187:G>A
ADCY1
NM_021116:c.639+1406G>A
INTRON1
Unknown significance
rs562960145
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
0
694
0
3
1008
0.003
0
978
0
3
5008
0.000599042
762892
chr7:45616198:C>G
ADCY1
NM_021116:c.639+1417C>G
INTRON1
Unknown significance
rs530409969
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
762893
chr7:45616213:G>T
ADCY1
NM_021116:c.639+1432G>T
INTRON1
Unknown significance
rs376098725
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
762894
chr7:45616214:C>A
ADCY1
NM_021116:c.639+1433C>A
INTRON1
Unknown significance
rs564404193
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
762895
chr7:45616226:C>T
ADCY1
NM_021116:c.639+1445C>T
INTRON1
Unknown significance
rs528317772
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
762896
chr7:45616241:C>T
ADCY1
NM_021116:c.639+1460C>T
INTRON1
Unknown significance
rs780587291
This variant is a VUS because it does not have enough information.
762897
chr7:45616280:A>G
ADCY1
NM_021116:c.639+1499A>G
INTRON1
Benign
rs58500623
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
3
694
0.0043
0
1008
0
0
978
0
15
5008
0.00299521
762898
chr7:45616293:T>A
ADCY1
NM_021116:c.639+1512T>A
INTRON1
Unknown significance
rs568216723
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
762899
chr7:45616301:C>G
ADCY1
NM_021116:c.639+1520C>G
INTRON1
Unknown significance
rs536762838
This variant is a VUS because it does not have enough information.
1
1322
0.0008
0
1006
0
1
694
0.0014
0
1008
0
0
978
0
2
5008
0.000399361
762900
chr7:45616334:G>C
ADCY1
NM_021116:c.639+1553G>C
INTRON1
Unknown significance
rs548664887
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
762901
chr7:45616336:C>-
ADCY1
NM_021116:c.639+1555delC
INTRON1
Unknown significance
rs747452045
This variant is a VUS because it does not have enough information.
762902
chr7:45616352:C>T
ADCY1
NM_021116:c.639+1571C>T
INTRON1
Unknown significance
rs542371643
This variant is a VUS because it does not have enough information.
762903
chr7:45616365:C>T
ADCY1
NM_021116:c.639+1584C>T
INTRON1
Unknown significance
rs140090608
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
762904
chr7:45616382:C>T
ADCY1
NM_021116:c.639+1601C>T
INTRON1
Unknown significance
rs747663179
This variant is a VUS because it does not have enough information.
762905
chr7:45616478:C>T
ADCY1
NM_021116:c.639+1697C>T
INTRON1
Unknown significance
rs563745525
This variant is a VUS because it does not have enough information.
762906
chr7:45616494:G>C
ADCY1
NM_021116:c.639+1713G>C
INTRON1
Unknown significance
rs767923548
This variant is a VUS because it does not have enough information.
762907
chr7:45616504:G>C
ADCY1
NM_021116:c.639+1723G>C
INTRON1
Benign
rs6977779
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
14
1322
0.0106
0
1006
0
0
694
0
0
1008
0
0
978
0
14
5008
0.00279553
762908
chr7:45616504:G>T
ADCY1
NM_021116:c.639+1723G>T
INTRON1
Unknown significance
rs6977779
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
762909
chr7:45616509:G>A
ADCY1
NM_021116:c.639+1728G>A
INTRON1
Unknown significance
rs750892273
This variant is a VUS because it does not have enough information.
762910
chr7:45616537:A>G
ADCY1
NM_021116:c.639+1756A>G
INTRON1
Benign
rs75813508
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
63
1322
0.0477
19
1006
0.0189
10
694
0.0144
26
1008
0.0258
36
978
0.0368
154
5008
0.0307508
762911
chr7:45616541:T>G
ADCY1
NM_021116:c.639+1760T>G
INTRON1
Unknown significance
rs765935242
This variant is a VUS because it does not have enough information.
762912
chr7:45616563:T>G
ADCY1
NM_021116:c.639+1782T>G
INTRON1
Unknown significance
rs186754300
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
762913
chr7:45616612:A>G
ADCY1
NM_021116:c.639+1831A>G
INTRON1
Unknown significance
rs553153862
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
762914
chr7:45616674:G>C
ADCY1
NM_021116:c.639+1893G>C
INTRON1
Unknown significance
rs574658249
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
762915
chr7:45616676:C>T
ADCY1
NM_021116:c.639+1895C>T
INTRON1
Unknown significance
rs190117847
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
762916
chr7:45616694:A>G
ADCY1
NM_021116:c.639+1913A>G
INTRON1
Benign
rs150023156
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
14
1322
0.0106
0
1006
0
0
694
0
1
1008
0.001
0
978
0
15
5008
0.00299521
762917
chr7:45616736:G>T
ADCY1
NM_021116:c.639+1955G>T
INTRON1
Unknown significance
rs574942411
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
762918
chr7:45616761:T>C
ADCY1
NM_021116:c.639+1980T>C
INTRON1
Unknown significance
rs762528898
This variant is a VUS because it does not have enough information.
762919
chr7:45616772:A>G
ADCY1
NM_021116:c.639+1991A>G
INTRON1
Unknown significance
rs545775759
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
762920
chr7:45616774:G>A
ADCY1
NM_021116:c.639+1993G>A
INTRON1
Unknown significance
rs563887572
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
762921
chr7:45616812:A>G
ADCY1
NM_021116:c.639+2031A>G
INTRON1
Unknown significance
rs145343321
This variant is a VUS because it does not have enough information.
4
1322
0.003
0
1006
0
1
694
0.0014
0
1008
0
0
978
0
5
5008
0.000998403
762922
chr7:45616861:A>G
ADCY1
NM_021116:c.639+2080A>G
INTRON1
Unknown significance
rs753373655
This variant is a VUS because it does not have enough information.
762923
chr7:45616873:C>G
ADCY1
NM_021116:c.639+2092C>G
INTRON1
Unknown significance
rs540125037
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
762924
chr7:45616898:A>G
ADCY1
NM_021116:c.639+2117A>G
INTRON1
Unknown significance
rs561883607
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
762925
chr7:45616909:C>T
ADCY1
NM_021116:c.639+2128C>T
INTRON1
Unknown significance
rs574109465
This variant is a VUS because it does not have enough information.
762926
chr7:45616935:T>C
ADCY1
NM_021116:c.639+2154T>C
INTRON1
Unknown significance
rs770695831
This variant is a VUS because it does not have enough information.
762927
chr7:45616947:->G
ADCY1
NM_021116:c.639+2166_639+2167insG
INTRON1
Unknown significance
rs34673212
This variant is a VUS because it does not have enough information.
762928
chr7:45616951:A>T
ADCY1
NM_021116:c.639+2170A>T
INTRON1
Unknown significance
rs778626987
This variant is a VUS because it does not have enough information.
762929
chr7:45616955:A>G
ADCY1
NM_021116:c.639+2174A>G
INTRON1
Unknown significance
rs529087120
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
762930
chr7:45616966:C>T
ADCY1
NM_021116:c.639+2185C>T
INTRON1
Unknown significance
rs371472241
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
762931
chr7:45616970:C>G
ADCY1
NM_021116:c.639+2189C>G
INTRON1
Unknown significance
rs752495516
This variant is a VUS because it does not have enough information.
762932
chr7:45616999:A>G
ADCY1
NM_021116:c.639+2218A>G
INTRON1
Benign
rs149228627
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
4
1322
0.003
28
1006
0.0278
5
694
0.0072
10
1008
0.0099
101
978
0.1033
148
5008
0.0295527
762933
chr7:45617009:C>T
ADCY1
NM_021116:c.639+2228C>T
INTRON1
Unknown significance
rs530852227
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
762934
chr7:45617015:A>G
ADCY1
NM_021116:c.639+2234A>G
INTRON1
Unknown significance
rs552551538
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
762935
chr7:45617059:T>C
ADCY1
NM_021116:c.639+2278T>C
INTRON1
Unknown significance
rs570710669
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
762936
chr7:45617060:C>T
ADCY1
NM_021116:c.639+2279C>T
INTRON1
Unknown significance
rs777580844
This variant is a VUS because it does not have enough information.
762937
chr7:45617094:G>A
ADCY1
NM_021116:c.639+2313G>A
INTRON1
Unknown significance
rs535601658
This variant is a VUS because it does not have enough information.
762938
chr7:45617109:C>T
ADCY1
NM_021116:c.639+2328C>T
INTRON1
Unknown significance
rs369207439
This variant is a VUS because it does not have enough information.
762939
chr7:45617130:T>C
ADCY1
NM_021116:c.639+2349T>C
INTRON1
Benign
rs535349622
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
762940
chr7:45617131:C>T
ADCY1
NM_021116:c.639+2350C>T
INTRON1
Benign
rs143386069
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
14
1008
0.0139
0
978
0
14
5008
0.00279553
762941
chr7:45617192:G>A
ADCY1
NM_021116:c.639+2411G>A
INTRON1
Unknown significance
rs568342942
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
762942
chr7:45617279:A>G
ADCY1
NM_021116:c.639+2498A>G
INTRON1
Unknown significance
rs535648638
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
762943
chr7:45617293:C>T
ADCY1
NM_021116:c.639+2512C>T
INTRON1
Unknown significance
rs556678018
This variant is a VUS because it does not have enough information.
2
1322
0.0015
0
1006
0
1
694
0.0014
0
1008
0
0
978
0
3
5008
0.000599042
762944
chr7:45617319:C>G
ADCY1
NM_021116:c.639+2538C>G
INTRON1
Unknown significance
rs769885334
This variant is a VUS because it does not have enough information.
762945
chr7:45617372:T>A
ADCY1
NM_021116:c.639+2591T>A
INTRON1
Unknown significance
rs759466494
This variant is a VUS because it does not have enough information.
762946
chr7:45617383:T>G
ADCY1
NM_021116:c.639+2602T>G
INTRON1
Benign
rs78338109
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
0
1322
0
1
1006
0.001
15
694
0.0216
125
1008
0.124
34
978
0.0348
175
5008
0.0349441
762947
chr7:45617405:C>T
ADCY1
NM_021116:c.639+2624C>T
INTRON1
Benign
rs115342333
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
0
694
0
0
1008
0
0
978
0
13
5008
0.00259585
762948
chr7:45617408:G>T
ADCY1
NM_021116:c.639+2627G>T
INTRON1
Unknown significance
rs749336657
This variant is a VUS because it does not have enough information.
762949
chr7:45617422:G>A
ADCY1
NM_021116:c.639+2641G>A
INTRON1
Unknown significance
rs557753945
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
762950
chr7:45617433:C>T
ADCY1
NM_021116:c.639+2652C>T
INTRON1
Benign
rs115787895
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
11
1322
0.0083
0
1006
0
0
694
0
0
1008
0
0
978
0
11
5008
0.00219649
762951
chr7:45617472:G>A
ADCY1
NM_021116:c.639+2691G>A
INTRON1
Unknown significance
rs768817045
This variant is a VUS because it does not have enough information.
762952
chr7:45617488:T>A
ADCY1
NM_021116:c.639+2707T>A
INTRON1
Unknown significance
rs181405465
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
762953
chr7:45617493:C>A
ADCY1
NM_021116:c.639+2712C>A
INTRON1
Unknown significance
rs752707760
This variant is a VUS because it does not have enough information.
762954
chr7:45617513:C>T
ADCY1
NM_021116:c.639+2732C>T
INTRON1
Unknown significance
rs774574445
This variant is a VUS because it does not have enough information.
762955
chr7:45617518:G>A
ADCY1
NM_021116:c.639+2737G>A
INTRON1
Benign
rs185937564
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
762956
chr7:45617536:T>A
ADCY1
NM_021116:c.639+2755T>A
INTRON1
Unknown significance
rs760771734
This variant is a VUS because it does not have enough information.
762957
chr7:45617565:G>A
ADCY1
NM_021116:c.639+2784G>A
INTRON1
Unknown significance
rs529150659
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
762958
chr7:45617596:C>A
ADCY1
NM_021116:c.639+2815C>A
INTRON1
Unknown significance
rs544412603
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
762959
chr7:45617628:G>A
ADCY1
NM_021116:c.639+2847G>A
INTRON1
Benign
rs79268889
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
0
1322
0
1
1006
0.001
15
694
0.0216
125
1008
0.124
34
978
0.0348
175
5008
0.0349441
762960
chr7:45617630:A>G
ADCY1
NM_021116:c.639+2849A>G
INTRON1
Unknown significance
rs201513838
This variant is a VUS because it does not have enough information.
762961
chr7:45617640:C>G
ADCY1
NM_021116:c.639+2859C>G
INTRON1
Unknown significance
rs531037916
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
762962
chr7:45617661:C>G
ADCY1
NM_021116:c.639+2880C>G
INTRON1
Unknown significance
rs552361512
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
762963
chr7:45617698:C>T
ADCY1
NM_021116:c.639+2917C>T
INTRON1
Unknown significance
rs146795025
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
762964
chr7:45617722:C>T
ADCY1
NM_021116:c.639+2941C>T
INTRON1
Unknown significance
rs528453192
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
762965
chr7:45617752:G>C
ADCY1
NM_021116:c.639+2971G>C
INTRON1
Unknown significance
rs772437596
This variant is a VUS because it does not have enough information.
762966
chr7:45617815:C>T
ADCY1
NM_021116:c.639+3034C>T
INTRON1
Unknown significance
rs773874157
This variant is a VUS because it does not have enough information.
762967
chr7:45617845:C>T
ADCY1
NM_021116:c.639+3064C>T
INTRON1
Unknown significance
rs546935477
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
762968
chr7:45617859:C>A
ADCY1
NM_021116:c.639+3078C>A
INTRON1
Unknown significance
rs761311232
This variant is a VUS because it does not have enough information.
762969
chr7:45617862:T>G
ADCY1
NM_021116:c.639+3081T>G
INTRON1
Unknown significance
rs568403788
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
762970
chr7:45617881:C>A
ADCY1
NM_021116:c.639+3100C>A
INTRON1
Unknown significance
rs535708478
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
762971
chr7:45617893:G>A
ADCY1
NM_021116:c.639+3112G>A
INTRON1
Unknown significance
rs140481106
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
762972
chr7:45617901:->G
ADCY1
NM_021116:c.639+3120_639+3121insG
INTRON1
Benign
rs565184011
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
11
1322
0.0083
1
1006
0.001
1
694
0.0014
0
1008
0
0
978
0
13
5008
0.00259585
762974
chr7:45617901:G>A
ADCY1
NM_021116:c.639+3120G>A
INTRON1
Unknown significance
rs77226271
This variant is a VUS because it does not have enough information.
762973
chr7:45617901:G>T
ADCY1
NM_021116:c.639+3120G>T
INTRON1
Unknown significance
rs77226271
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
762975
chr7:45617902:G>C
ADCY1
NM_021116:c.639+3121G>C
INTRON1
Unknown significance
rs766959182
This variant is a VUS because it does not have enough information.
762976
chr7:45617937:A>G
ADCY1
NM_021116:c.639+3156A>G
INTRON1
Unknown significance
rs539532212
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
762977
chr7:45617981:A>G
ADCY1
NM_021116:c.639+3200A>G
INTRON1
Benign
rs10807926
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
461
1322
0.3487
448
1006
0.4453
264
694
0.3804
514
1008
0.5099
499
978
0.5102
2186
5008
0.436502
762978
chr7:45617997:C>A
ADCY1
NM_021116:c.639+3216C>A
INTRON1
Unknown significance
rs572826798
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
762979
chr7:45618001:C>G
ADCY1
NM_021116:c.639+3220C>G
INTRON1
Unknown significance
rs759076039
This variant is a VUS because it does not have enough information.
762980
chr7:45618005:C>T
ADCY1
NM_021116:c.639+3224C>T
INTRON1
Benign
rs10951823
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
473
1322
0.3578
478
1006
0.4751
286
694
0.4121
672
1008
0.6667
603
978
0.6166
2512
5008
0.501597
762981
chr7:45618083:G>C
ADCY1
NM_021116:c.639+3302G>C
INTRON1
Benign
rs10951824
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
177
1322
0.1339
351
1006
0.3489
220
694
0.317
474
1008
0.4702
355
978
0.363
1577
5008
0.314896
762982
chr7:45618116:T>C
ADCY1
NM_021116:c.639+3335T>C
INTRON1
Unknown significance
rs573994197
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
762983
chr7:45618151:G>A
ADCY1
NM_021116:c.639+3370G>A
INTRON1
Unknown significance
rs544472918
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
762984
chr7:45618182:T>C
ADCY1
NM_021116:c.639+3401T>C
INTRON1
Unknown significance
rs371761404
This variant is a VUS because it does not have enough information.
762985
chr7:45618230:G>T
ADCY1
NM_021116:c.639+3449G>T
INTRON1
Unknown significance
rs562725069
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
762986
chr7:45618273:G>T
ADCY1
NM_021116:c.639+3492G>T
INTRON1
Unknown significance
rs145709267
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
762987
chr7:45618288:C>A
ADCY1
NM_021116:c.639+3507C>A
INTRON1
Unknown significance
rs138278818
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
762988
chr7:45618303:C>T
ADCY1
NM_021116:c.639+3522C>T
INTRON1
Unknown significance
rs568106690
This variant is a VUS because it does not have enough information.
762989
chr7:45618304:G>A
ADCY1
NM_021116:c.639+3523G>A
INTRON1
Unknown significance
rs564419630
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
762990
chr7:45618320:C>T
ADCY1
NM_021116:c.639+3539C>T
INTRON1
Unknown significance
rs548347333
This variant is a VUS because it does not have enough information.
762991
chr7:45618347:G>A
ADCY1
NM_021116:c.639+3566G>A
INTRON1
Unknown significance
rs528526674
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
0
694
0
3
1008
0.003
0
978
0
3
5008
0.000599042
762992
chr7:45618363:A>G
ADCY1
NM_021116:c.639+3582A>G
INTRON1
Unknown significance
rs546596897
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
762993
chr7:45618378:C>A
ADCY1
NM_021116:c.639+3597C>A
INTRON1
Unknown significance
rs751334807
This variant is a VUS because it does not have enough information.
762994
chr7:45618390:T>A
ADCY1
NM_021116:c.639+3609T>A
INTRON1
Unknown significance
rs757226648
This variant is a VUS because it does not have enough information.
762996
chr7:45618396:T>G
ADCY1
NM_021116:c.639+3615T>G
INTRON1
Unknown significance
rs561698330
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
762995
chr7:45618396:TCC>-
ADCY1
NM_021116:c.639+3615_639+3617delTCC
INTRON1
Unknown significance
rs796924130
This variant is a VUS because it does not have enough information.
762997
chr7:45618407:C>G
ADCY1
NM_021116:c.639+3626C>G
INTRON1
Unknown significance
rs781092341
This variant is a VUS because it does not have enough information.
762998
chr7:45618416:T>C
ADCY1
NM_021116:c.639+3635T>C
INTRON1
Unknown significance
rs529562852
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
762999
chr7:45618436:C>T
ADCY1
NM_021116:c.639+3655C>T
INTRON1
Unknown significance
rs190789844
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
763000
chr7:45618439:C>G
ADCY1
NM_021116:c.639+3658C>G
INTRON1
Benign
rs4529350
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
213
1322
0.1611
78
1006
0.0775
34
694
0.049
10
1008
0.0099
108
978
0.1104
443
5008
0.0884585
763001
chr7:45618442:T>G
ADCY1
NM_021116:c.639+3661T>G
INTRON1
Unknown significance
rs569788915
This variant is a VUS because it does not have enough information.
763002
chr7:45618458:C>T
ADCY1
NM_021116:c.639+3677C>T
INTRON1
Unknown significance
rs780489296
This variant is a VUS because it does not have enough information.
763003
chr7:45618481:->T
ADCY1
NM_021116:c.639+3700_639+3701insT
INTRON1
Unknown significance
rs35406812
This variant is a VUS because it does not have enough information.
763004
chr7:45618492:A>G
ADCY1
NM_021116:c.639+3711A>G
INTRON1
Benign
rs141736735
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
15
1008
0.0149
2
978
0.002
17
5008
0.00339457
763005
chr7:45618513:T>C
ADCY1
NM_021116:c.639+3732T>C
INTRON1
Benign
rs78344730
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
0
1322
0
1
1006
0.001
15
694
0.0216
125
1008
0.124
34
978
0.0348
175
5008
0.0349441
763006
chr7:45618531:T>G
ADCY1
NM_021116:c.639+3750T>G
INTRON1
Unknown significance
rs547084374
This variant is a VUS because it does not have enough information.
763007
chr7:45618538:C>T
ADCY1
NM_021116:c.639+3757C>T
INTRON1
Unknown significance
rs748349744
This variant is a VUS because it does not have enough information.
763008
chr7:45618558:G>A
ADCY1
NM_021116:c.639+3777G>A
INTRON1
Unknown significance
rs772158709
This variant is a VUS because it does not have enough information.
763009
chr7:45618570:T>G
ADCY1
NM_021116:c.639+3789T>G
INTRON1
Benign
rs184169017
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
763010
chr7:45618622:C>T
ADCY1
NM_021116:c.639+3841C>T
INTRON1
Benign
rs74698704
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
9
1322
0.0068
29
1006
0.0288
7
694
0.0101
37
1008
0.0367
67
978
0.0685
149
5008
0.0297524
763011
chr7:45618631:G>A
ADCY1
NM_021116:c.639+3850G>A
INTRON1
Benign
rs187561557
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
763012
chr7:45618640:C>G
ADCY1
NM_021116:c.639+3859C>G
INTRON1
Unknown significance
rs150153106
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
763013
chr7:45618671:C>T
ADCY1
NM_021116:c.639+3890C>T
INTRON1
Unknown significance
rs59442380
This variant is a VUS because it does not have enough information.
763014
chr7:45618690:C>T
ADCY1
NM_021116:c.639+3909C>T
INTRON1
Unknown significance
rs538153526
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
763015
chr7:45618732:C>T
ADCY1
NM_021116:c.639+3951C>T
INTRON1
Benign
rs79515181
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
9
1322
0.0068
29
1006
0.0288
7
694
0.0101
37
1008
0.0367
67
978
0.0685
149
5008
0.0297524
763016
chr7:45618737:A>C
ADCY1
NM_021116:c.639+3956A>C
INTRON1
Unknown significance
rs577814302
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
763017
chr7:45618746:G>T
ADCY1
NM_021116:c.639+3965G>T
INTRON1
Unknown significance
rs771626361
This variant is a VUS because it does not have enough information.
763018
chr7:45618751:A>G
ADCY1
NM_021116:c.639+3970A>G
INTRON1
Unknown significance
rs569784709
This variant is a VUS because it does not have enough information.
763019
chr7:45618786:T>C
ADCY1
NM_021116:c.639+4005T>C
INTRON1
Unknown significance
rs138584557
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
763020
chr7:45618788:G>A
ADCY1
NM_021116:c.639+4007G>A
INTRON1
Benign
rs76835720
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
63
1322
0.0477
19
1006
0.0189
10
694
0.0144
26
1008
0.0258
36
978
0.0368
154
5008
0.0307508
763021
chr7:45618802:C>T
ADCY1
NM_021116:c.639+4021C>T
INTRON1
Unknown significance
rs149333919
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
763022
chr7:45618823:A>G
ADCY1
NM_021116:c.639+4042A>G
INTRON1
Unknown significance
rs540300058
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
763023
chr7:45618826:C>T
ADCY1
NM_021116:c.639+4045C>T
INTRON1
Unknown significance
rs561759734
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
763024
chr7:45618842:G>A
ADCY1
NM_021116:c.639+4061G>A
INTRON1
Unknown significance
rs191203239
This variant is a VUS because it does not have enough information.
0
1322
0
3
1006
0.003
0
694
0
0
1008
0
0
978
0
3
5008
0.000599042
763025
chr7:45618867:A>C
ADCY1
NM_021116:c.639+4086A>C
INTRON1
Unknown significance
rs551288572
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
763026
chr7:45618868:C>G
ADCY1
NM_021116:c.639+4087C>G
INTRON1
Benign
rs76323096
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
18
1322
0.0136
0
1006
0
0
694
0
0
1008
0
0
978
0
18
5008
0.00359425
763027
chr7:45618882:G>A
ADCY1
NM_021116:c.639+4101G>A
INTRON1
Unknown significance
rs111244229
This variant is a VUS because it does not have enough information.
763028
chr7:45618958:G>T
ADCY1
NM_021116:c.639+4177G>T
INTRON1
Unknown significance
rs533617804
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
763029
chr7:45618962:C>T
ADCY1
NM_021116:c.639+4181C>T
INTRON1
Unknown significance
rs551694790
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
763030
chr7:45618986:C>T
ADCY1
NM_021116:c.639+4205C>T
INTRON1
Unknown significance
rs567009174
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
763031
chr7:45618987:G>C
ADCY1
NM_021116:c.639+4206G>C
INTRON1
Unknown significance
rs527405220
This variant is a VUS because it does not have enough information.
1
1322
0.0008
0
1006
0
1
694
0.0014
0
1008
0
0
978
0
2
5008
0.000399361
763033
chr7:45619019:C>G
ADCY1
NM_021116:c.639+4238C>G
INTRON1
Unknown significance
rs549066278
This variant is a VUS because it does not have enough information.
763032
chr7:45619019:C>T
ADCY1
NM_021116:c.639+4238C>T
INTRON1
Unknown significance
rs549066278
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
763034
chr7:45619031:T>C
ADCY1
NM_021116:c.639+4250T>C
INTRON1
Benign
rs867582
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
457
1322
0.3457
448
1006
0.4453
264
694
0.3804
510
1008
0.506
499
978
0.5102
2178
5008
0.434904
763035
chr7:45619072:C>A
ADCY1
NM_021116:c.639+4291C>A
INTRON1
Unknown significance
rs537837202
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
763036
chr7:45619083:C>T
ADCY1
NM_021116:c.639+4302C>T
INTRON1
Unknown significance
rs556461975
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
763037
chr7:45619111:C>T
ADCY1
NM_021116:c.639+4330C>T
INTRON1
Unknown significance
rs368508495
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
763038
chr7:45619116:A>G
ADCY1
NM_021116:c.639+4335A>G
INTRON1
Unknown significance
rs182576149
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
763039
chr7:45619119:T>C
ADCY1
NM_021116:c.639+4338T>C
INTRON1
Benign
rs2877339
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
490
1322
0.3707
478
1006
0.4751
286
694
0.4121
672
1008
0.6667
603
978
0.6166
2529
5008
0.504992
763040
chr7:45619169:C>A
ADCY1
NM_021116:c.639+4388C>A
INTRON1
Unknown significance
rs372822877
This variant is a VUS because it does not have enough information.
763041
chr7:45619200:C>T
ADCY1
NM_021116:c.639+4419C>T
INTRON1
Unknown significance
rs187003728
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
763042
chr7:45619203:C>T
ADCY1
NM_021116:c.639+4422C>T
INTRON1
Unknown significance
rs540358183
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
763043
chr7:45619224:C>T
ADCY1
NM_021116:c.639+4443C>T
INTRON1
Unknown significance
rs537338513
This variant is a VUS because it does not have enough information.
763044
chr7:45619246:G>A
ADCY1
NM_021116:c.639+4465G>A
INTRON1
Benign
rs117074744
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
4
1322
0.003
29
1006
0.0288
5
694
0.0072
10
1008
0.0099
101
978
0.1033
149
5008
0.0297524
763045
chr7:45619250:T>G
ADCY1
NM_021116:c.639+4469T>G
INTRON1
Unknown significance
rs750334644
This variant is a VUS because it does not have enough information.
763046
chr7:45619360:G>A
ADCY1
NM_021116:c.639+4579G>A
INTRON1
Unknown significance
rs573747109
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
763047
chr7:45619362:C>A
ADCY1
NM_021116:c.639+4581C>A
INTRON1
Benign
rs114564186
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
1
694
0.0014
0
1008
0
0
978
0
11
5008
0.00219649
763048
chr7:45619380:T>A
ADCY1
NM_021116:c.639+4599T>A
INTRON1
Unknown significance
rs772027171
This variant is a VUS because it does not have enough information.
763049
chr7:45619440:G>A
ADCY1
NM_021116:c.639+4659G>A
INTRON1
Unknown significance
rs562862759
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
2
978
0.002
4
5008
0.000798722
763050
chr7:45619464:G>T
ADCY1
NM_021116:c.639+4683G>T
INTRON1
Unknown significance
rs533461200
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
763051
chr7:45619520:T>A
ADCY1
NM_021116:c.639+4739T>A
INTRON1
Benign
rs1879591
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
0
1322
0
1
1006
0.001
15
694
0.0216
125
1008
0.124
34
978
0.0348
175
5008
0.0349441
763052
chr7:45619542:C>T
ADCY1
NM_021116:c.639+4761C>T
INTRON1
Unknown significance
rs560684379
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
763053
chr7:45619545:C>-
ADCY1
NM_021116:c.639+4764delC
INTRON1
Unknown significance
rs752619537
This variant is a VUS because it does not have enough information.
763054
chr7:45619551:C>T
ADCY1
NM_021116:c.639+4770C>T
INTRON1
Unknown significance
rs558892121
This variant is a VUS because it does not have enough information.
763055
chr7:45619557:C>G
ADCY1
NM_021116:c.639+4776C>G
INTRON1
Benign
rs527871872
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
763056
chr7:45619561:C>A
ADCY1
NM_021116:c.639+4780C>A
INTRON1
Unknown significance
rs71537753
This variant is a VUS because it does not have enough information.
763057
chr7:45619569:G>C
ADCY1
NM_021116:c.639+4788G>C
INTRON1
Unknown significance
rs867516
This variant is a VUS because it does not have enough information.
763058
chr7:45619590:G>A
ADCY1
NM_021116:c.639+4809G>A
INTRON1
Benign
rs116636770
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
1
694
0.0014
0
1008
0
0
978
0
13
5008
0.00259585
763059
chr7:45619694:A>C
ADCY1
NM_021116:c.639+4913A>C
INTRON1
Unknown significance
rs139481487
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
763060
chr7:45619706:A>G
ADCY1
NM_021116:c.639+4925A>G
INTRON1
Unknown significance
rs375927852
This variant is a VUS because it does not have enough information.
763061
chr7:45619743:G>A
ADCY1
NM_021116:c.639+4962G>A
INTRON1
Unknown significance
rs531394989
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
763062
chr7:45619764:G>A
ADCY1
NM_021116:c.639+4983G>A
INTRON1
Unknown significance
rs779095183
This variant is a VUS because it does not have enough information.
763063
chr7:45619771:G>C
ADCY1
NM_021116:c.639+4990G>C
INTRON1
Unknown significance
rs576866878
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
763064
chr7:45619805:G>T
ADCY1
NM_021116:c.639+5024G>T
INTRON1
Unknown significance
rs748142473
This variant is a VUS because it does not have enough information.
763065
chr7:45619848:C>A
ADCY1
NM_021116:c.639+5067C>A
INTRON1
Unknown significance
rs758757538
This variant is a VUS because it does not have enough information.
763066
chr7:45619852:G>T
ADCY1
NM_021116:c.639+5071G>T
INTRON1
Unknown significance
rs571193077
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
763067
chr7:45619868:G>T
ADCY1
NM_021116:c.639+5087G>T
INTRON1
Unknown significance
rs535598024
This variant is a VUS because it does not have enough information.
763068
chr7:45619903:T>C
ADCY1
NM_021116:c.639+5122T>C
INTRON1
Unknown significance
rs143374629
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
763069
chr7:45619941:T>A
ADCY1
NM_021116:c.639+5160T>A
INTRON1
Unknown significance
rs778130897
This variant is a VUS because it does not have enough information.
763070
chr7:45619970:AG>-
ADCY1
NM_021116:c.639+5189_639+5190delAG
INTRON1
Benign
rs563791445
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
7
978
0.0072
7
5008
0.00139776
763071
chr7:45619971:G>T
ADCY1
NM_021116:c.639+5190G>T
INTRON1
Unknown significance
rs554015132
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
763072
chr7:45620020:C>T
ADCY1
NM_021116:c.639+5239C>T
INTRON1
Benign
rs191834124
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
1
694
0.0014
0
1008
0
0
978
0
13
5008
0.00259585
763073
chr7:45620031:A>G
ADCY1
NM_021116:c.639+5250A>G
INTRON1
Unknown significance
rs147166821
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
763074
chr7:45620094:C>T
ADCY1
NM_021116:c.639+5313C>T
INTRON1
Unknown significance
rs764152495
This variant is a VUS because it does not have enough information.
763075
chr7:45620114:T>C
ADCY1
NM_021116:c.639+5333T>C
INTRON1
Unknown significance
rs555483733
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
763076
chr7:45620123:C>A
ADCY1
NM_021116:c.639+5342C>A
INTRON1
Unknown significance
rs557509592
This variant is a VUS because it does not have enough information.
763077
chr7:45620129:T>A
ADCY1
NM_021116:c.639+5348T>A
INTRON1
Unknown significance
rs776571194
This variant is a VUS because it does not have enough information.
763078
chr7:45620138:C>G
ADCY1
NM_021116:c.639+5357C>G
INTRON1
Unknown significance
rs771358741
This variant is a VUS because it does not have enough information.
763079
chr7:45620221:C>T
ADCY1
NM_021116:c.639+5440C>T
INTRON1
Benign
rs575945033
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
0
1322
0
1
1006
0.001
1
694
0.0014
0
1008
0
8
978
0.0082
10
5008
0.00199681
763080
chr7:45620228:C>T
ADCY1
NM_021116:c.639+5447C>T
INTRON1
Unknown significance
rs746338322
This variant is a VUS because it does not have enough information.
763081
chr7:45620241:C>T
ADCY1
NM_021116:c.639+5460C>T
INTRON1
Unknown significance
rs544648503
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
763082
chr7:45620282:G>A
ADCY1
NM_021116:c.639+5501G>A
INTRON1
Benign
rs79597784
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
63
1322
0.0477
19
1006
0.0189
10
694
0.0144
27
1008
0.0268
36
978
0.0368
155
5008
0.0309505
763083
chr7:45620286:G>A
ADCY1
NM_021116:c.639+5505G>A
INTRON1
Benign
rs79941245
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
63
1322
0.0477
19
1006
0.0189
10
694
0.0144
27
1008
0.0268
36
978
0.0368
155
5008
0.0309505
763084
chr7:45620306:C>T
ADCY1
NM_021116:c.639+5525C>T
INTRON1
Benign
rs140445635
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
11
1322
0.0083
0
1006
0
0
694
0
0
1008
0
0
978
0
11
5008
0.00219649
763085
chr7:45620310:A>T
ADCY1
NM_021116:c.639+5529A>T
INTRON1
Unknown significance
rs184426057
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
763086
chr7:45620313:G>T
ADCY1
NM_021116:c.639+5532G>T
INTRON1
Unknown significance
rs573588083
This variant is a VUS because it does not have enough information.
763087
chr7:45620321:G>-
ADCY1
NM_021116:c.639+5540delG
INTRON1
Unknown significance
rs370784954
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
763088
chr7:45620324:G>A
ADCY1
NM_021116:c.639+5543G>A
INTRON1
Unknown significance
rs142108148
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
763089
chr7:45620324:G>T
ADCY1
NM_021116:c.639+5543G>T
INTRON1
Unknown significance
rs142108148
This variant is a VUS because it does not have enough information.
763090
chr7:45620343:T>C
ADCY1
NM_021116:c.639+5562T>C
INTRON1
Unknown significance
rs543253027
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
763091
chr7:45620348:C>G
ADCY1
NM_021116:c.639+5567C>G
INTRON1
Benign
rs80276915
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
51
1322
0.0386
0
1006
0
2
694
0.0029
0
1008
0
0
978
0
53
5008
0.0105831
763092
chr7:45620363:A>G
ADCY1
NM_021116:c.639+5582A>G
INTRON1
Unknown significance
rs773925007
This variant is a VUS because it does not have enough information.
763093
chr7:45620383:G>A
ADCY1
NM_021116:c.639+5602G>A
INTRON1
Unknown significance
rs540191334
This variant is a VUS because it does not have enough information.
763094
chr7:45620385:->ATCT
ADCY1
NM_021116:c.639+5604_639+5605insATCT
INTRON1
Unknown significance
rs371227177
This variant is a VUS because it does not have enough information.
763095
chr7:45620393:G>A
ADCY1
NM_021116:c.639+5612G>A
INTRON1
Unknown significance
rs531327443
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
763096
chr7:45620420:->A
ADCY1
NM_021116:c.639+5639_639+5640insA
INTRON1
Unknown significance
rs35760107
This variant is a VUS because it does not have enough information.
763097
chr7:45620441:C>T
ADCY1
NM_021116:c.639+5660C>T
INTRON1
Unknown significance
rs767251105
This variant is a VUS because it does not have enough information.
763098
chr7:45620455:C>T
ADCY1
NM_021116:c.639+5674C>T
INTRON1
Unknown significance
rs549811766
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
763099
chr7:45620462:C>T
ADCY1
NM_021116:c.639+5681C>T
INTRON1
Unknown significance
rs750159088
This variant is a VUS because it does not have enough information.
763100
chr7:45620491:TGCC>-
ADCY1
NM_021116:c.639+5710_639+5713delTGCC
INTRON1
Unknown significance
rs371795946
This variant is a VUS because it does not have enough information.
763101
chr7:45620521:T>C
ADCY1
NM_021116:c.639+5740T>C
INTRON1
Unknown significance
rs187606844
This variant is a VUS because it does not have enough information.
763102
chr7:45620522:A>G
ADCY1
NM_021116:c.639+5741A>G
INTRON1
Unknown significance
rs193068873
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
763103
chr7:45620541:G>A
ADCY1
NM_021116:c.639+5760G>A
INTRON1
Unknown significance
rs766219065
This variant is a VUS because it does not have enough information.
763104
chr7:45620552:G>C
ADCY1
NM_021116:c.639+5771G>C
INTRON1
Benign
rs114233764
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
763105
chr7:45620591:G>C
ADCY1
NM_021116:c.639+5810G>C
INTRON1
Unknown significance
rs752044433
This variant is a VUS because it does not have enough information.
763106
chr7:45620595:C>T
ADCY1
NM_021116:c.639+5814C>T
INTRON1
Unknown significance
rs185852821
This variant is a VUS because it does not have enough information.
0
1322
0
0
1006
0
0
694
0
3
1008
0.003
0
978
0
3
5008
0.000599042
763107
chr7:45620616:C>G
ADCY1
NM_021116:c.639+5835C>G
INTRON1
Benign
rs77961100
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
37
1322
0.028
5
1006
0.005
4
694
0.0058
0
1008
0
0
978
0
46
5008
0.0091853
763108
chr7:45620620:G>A
ADCY1
NM_021116:c.639+5839G>A
INTRON1
Unknown significance
rs550436970
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
763109
chr7:45620640:C>T
ADCY1
NM_021116:c.639+5859C>T
INTRON1
Benign
rs115113253
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
11
1322
0.0083
1
1006
0.001
0
694
0
0
1008
0
0
978
0
12
5008
0.00239617
763110
chr7:45620649:G>A
ADCY1
NM_021116:c.639+5868G>A
INTRON1
Benign
rs58525807
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
42
1322
0.0318
38
1006
0.0378
22
694
0.0317
0
1008
0
9
978
0.0092
111
5008
0.0221645
763111
chr7:45620656:T>C
ADCY1
NM_021116:c.639+5875T>C
INTRON1
Unknown significance
rs757723467
This variant is a VUS because it does not have enough information.
763112
chr7:45620689:G>A
ADCY1
NM_021116:c.639+5908G>A
INTRON1
Unknown significance
rs537971013
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
763113
chr7:45620701:C>G
ADCY1
NM_021116:c.639+5920C>G
INTRON1
Benign
rs12670925
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
127
1322
0.0961
313
1006
0.3111
198
694
0.2853
472
1008
0.4683
346
978
0.3538
1456
5008
0.290735
763114
chr7:45620706:T>G
ADCY1
NM_021116:c.639+5925T>G
INTRON1
Unknown significance
rs577982154
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
763115
chr7:45620713:A>G
ADCY1
NM_021116:c.639+5932A>G
INTRON1
Unknown significance
rs369190555
This variant is a VUS because it does not have enough information.
763116
chr7:45620747:C>G
ADCY1
NM_021116:c.639+5966C>G
INTRON1
Unknown significance
rs746188255
This variant is a VUS because it does not have enough information.
763117
chr7:45620761:C>G
ADCY1
NM_021116:c.639+5980C>G
INTRON1
Unknown significance
rs547363273
This variant is a VUS because it does not have enough information.
763118
chr7:45620765:A>G
ADCY1
NM_021116:c.639+5984A>G
INTRON1
Unknown significance
rs539013911
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
763119
chr7:45620812:T>A
ADCY1
NM_021116:c.639+6031T>A
INTRON1
Unknown significance
rs770399700
This variant is a VUS because it does not have enough information.
763120
chr7:45620816:T>C
ADCY1
NM_021116:c.639+6035T>C
INTRON1
Unknown significance
rs554168582
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
763121
chr7:45620845:C>T
ADCY1
NM_021116:c.639+6064C>T
INTRON1
Unknown significance
rs572778842
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
763122
chr7:45620880:->CTA
ADCY1
NM_021116:c.639+6099_639+6100insCTA
INTRON1
Unknown significance
rs777482171
This variant is a VUS because it does not have enough information.
763123
chr7:45620884:C>G
ADCY1
NM_021116:c.639+6103C>G
INTRON1
Unknown significance
rs375212641
This variant is a VUS because it does not have enough information.
763124
chr7:45620884:C>T
ADCY1
NM_021116:c.639+6103C>T
INTRON1
Unknown significance
rs375212641
This variant is a VUS because it does not have enough information.
763125
chr7:45620891:C>T
ADCY1
NM_021116:c.639+6110C>T
INTRON1
Benign
rs116118686
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
35
1322
0.0265
0
1006
0
1
694
0.0014
0
1008
0
0
978
0
36
5008
0.0071885
763126
chr7:45620892:G>A
ADCY1
NM_021116:c.639+6111G>A
INTRON1
Unknown significance
rs748712550
This variant is a VUS because it does not have enough information.
763127
chr7:45620931:TAGT>-
ADCY1
NM_021116:c.639+6150_639+6153delTAGT
INTRON1
Unknown significance
rs571592698
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
763128
chr7:45620936:A>C
ADCY1
NM_021116:c.639+6155A>C
INTRON1
Unknown significance
rs139858012
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
763129
chr7:45620960:C>T
ADCY1
NM_021116:c.639+6179C>T
INTRON1
Benign
rs4724420
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
459
1322
0.3472
448
1006
0.4453
264
694
0.3804
508
1008
0.504
499
978
0.5102
2178
5008
0.434904
763130
chr7:45620969:C>T
ADCY1
NM_021116:c.639+6188C>T
INTRON1
Unknown significance
rs768114089
This variant is a VUS because it does not have enough information.
763131
chr7:45620974:C>T
ADCY1
NM_021116:c.639+6193C>T
INTRON1
Unknown significance
rs373398617
This variant is a VUS because it does not have enough information.
763132
chr7:45620987:C>A
ADCY1
NM_021116:c.639+6206C>A
INTRON1
Benign
rs6975096
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
63
1322
0.0477
19
1006
0.0189
10
694
0.0144
26
1008
0.0258
36
978
0.0368
154
5008
0.0307508
763133
chr7:45621025:C>T
ADCY1
NM_021116:c.639+6244C>T
INTRON1
Unknown significance
rs564987418
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
763134
chr7:45621031:C>T
ADCY1
NM_021116:c.639+6250C>T
INTRON1
Unknown significance
rs532054069
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
763135
chr7:45621045:T>C
ADCY1
NM_021116:c.639+6264T>C
INTRON1
Unknown significance
rs745523593
This variant is a VUS because it does not have enough information.
763136
chr7:45621090:C>T
ADCY1
NM_021116:c.639+6309C>T
INTRON1
Unknown significance
rs547001080
This variant is a VUS because it does not have enough information.
2
1322
0.0015
1
1006
0.001
0
694
0
0
1008
0
0
978
0
3
5008
0.000599042
763137
chr7:45621091:G>A
ADCY1
NM_021116:c.639+6310G>A
INTRON1
Unknown significance
rs189164930
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
763138
chr7:45621097:G>T
ADCY1
NM_021116:c.639+6316G>T
INTRON1
Unknown significance
rs761497962
This variant is a VUS because it does not have enough information.
763139
chr7:45621108:C>T
ADCY1
NM_021116:c.639+6327C>T
INTRON1
Unknown significance
rs569987185
This variant is a VUS because it does not have enough information.
763140
chr7:45621117:G>A
ADCY1
NM_021116:c.639+6336G>A
INTRON1
Benign
rs149857298
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
65
1322
0.0492
0
1006
0
2
694
0.0029
0
1008
0
0
978
0
67
5008
0.0133786
763141
chr7:45621188:G>T
ADCY1
NM_021116:c.639+6407G>T
INTRON1
Unknown significance
rs369660851
This variant is a VUS because it does not have enough information.
763142
chr7:45621233:C>T
ADCY1
NM_021116:c.639+6452C>T
INTRON1
Unknown significance
rs762300876
This variant is a VUS because it does not have enough information.
763143
chr7:45621238:C>A
ADCY1
NM_021116:c.639+6457C>A
INTRON1
Unknown significance
rs548047856
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
763144
chr7:45621245:C>T
ADCY1
NM_021116:c.639+6464C>T
INTRON1
Unknown significance
rs180684012
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
763145
chr7:45621267:T>G
ADCY1
NM_021116:c.639+6486T>G
INTRON1
Unknown significance
rs537229024
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
763146
chr7:45621278:C>T
ADCY1
NM_021116:c.639+6497C>T
INTRON1
Benign
rs79047754
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
2
1322
0.0015
46
1006
0.0457
28
694
0.0403
0
1008
0
3
978
0.0031
79
5008
0.0157748
763147
chr7:45621285:A>G
ADCY1
NM_021116:c.639+6504A>G
INTRON1
Unknown significance
rs568392630
This variant is a VUS because it does not have enough information.
763148
chr7:45621319:G>A
ADCY1
NM_021116:c.639+6538G>A
INTRON1
Unknown significance
rs766355112
This variant is a VUS because it does not have enough information.
763149
chr7:45621334:C>G
ADCY1
NM_021116:c.639+6553C>G
INTRON1
Unknown significance
rs571722278
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
763150
chr7:45621348:A>G
ADCY1
NM_021116:c.639+6567A>G
INTRON1
Unknown significance
rs534616817
This variant is a VUS because it does not have enough information.
0
1322
0
1
1006
0.001
1
694
0.0014
0
1008
0
4
978
0.0041
6
5008
0.00119808
763151
chr7:45621361:A>G
ADCY1
NM_021116:c.639+6580A>G
INTRON1
Unknown significance
rs554228178
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
763152
chr7:45621371:A>G
ADCY1
NM_021116:c.639+6590A>G
INTRON1
Unknown significance
rs146867738
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
763153
chr7:45621375:T>C
ADCY1
NM_021116:c.639+6594T>C
INTRON1
Benign
rs6957861
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
489
1322
0.3699
480
1006
0.4771
286
694
0.4121
670
1008
0.6647
603
978
0.6166
2528
5008
0.504792
763154
chr7:45621399:A>G
ADCY1
NM_021116:c.639+6618A>G
INTRON1
Unknown significance
rs575809669
This variant is a VUS because it does not have enough information.
763155
chr7:45621411:C>A
ADCY1
NM_021116:c.639+6630C>A
INTRON1
Unknown significance
rs764225388
This variant is a VUS because it does not have enough information.
763156
chr7:45621432:A>T
ADCY1
NM_021116:c.639+6651A>T
INTRON1
Unknown significance
rs555277758
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
2
978
0.002
4
5008
0.000798722
763157
chr7:45621436:A>G
ADCY1
NM_021116:c.639+6655A>G
INTRON1
Unknown significance
rs751667758
This variant is a VUS because it does not have enough information.
763158
chr7:45621438:A>G
ADCY1
NM_021116:c.639+6657A>G
INTRON1
Unknown significance
rs576603239
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
763159
chr7:45621444:->AC
ADCY1
NM_021116:c.639+6663_639+6664insAC
INTRON1
Unknown significance
rs770525738
This variant is a VUS because it does not have enough information.
763160
chr7:45621444:AC>-
ADCY1
NM_021116:c.639+6663_639+6664delAC
INTRON1
Unknown significance
rs769288579
This variant is a VUS because it does not have enough information.
763161
chr7:45621465:T>A
ADCY1
NM_021116:c.639+6684T>A
INTRON1
Unknown significance
rs543989873
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
763162
chr7:45621467:C>G
ADCY1
NM_021116:c.639+6686C>G
INTRON1
Benign
rs117687736
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
4
1322
0.003
28
1006
0.0278
5
694
0.0072
10
1008
0.0099
101
978
0.1033
148
5008
0.0295527
763163
chr7:45621467:C>T
ADCY1
NM_021116:c.639+6686C>T
INTRON1
Benign
rs117687736
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
763164
chr7:45621471:C>T
ADCY1
NM_021116:c.639+6690C>T
INTRON1
Unknown significance
rs781267519
This variant is a VUS because it does not have enough information.
763165
chr7:45621479:T>C
ADCY1
NM_021116:c.639+6698T>C
INTRON1
Benign
rs6958039
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
490
1322
0.3707
480
1006
0.4771
286
694
0.4121
670
1008
0.6647
603
978
0.6166
2529
5008
0.504992
763166
chr7:45621486:A>G
ADCY1
NM_021116:c.639+6705A>G
INTRON1
Unknown significance
rs558940399
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
763167
chr7:45621517:A>-
ADCY1
NM_021116:c.639+6736delA
INTRON1
Unknown significance
rs776680651
This variant is a VUS because it does not have enough information.
763168
chr7:45621523:G>C
ADCY1
NM_021116:c.639+6742G>C
INTRON1
Unknown significance
rs761831267
This variant is a VUS because it does not have enough information.
763169
chr7:45621527:G>A
ADCY1
NM_021116:c.639+6746G>A
INTRON1
Benign
rs117978250
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.
0
1322
0
1
1006
0.001
15
694
0.0216
125
1008
0.124
34
978
0.0348
175
5008
0.0349441
763170
chr7:45621534:A>G
ADCY1
NM_021116:c.639+6753A>G
INTRON1
Unknown significance
rs541750766
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
763171
chr7:45621587:A>G
ADCY1
NM_021116:c.639+6806A>G
INTRON1
Unknown significance
rs563596346
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
763172
chr7:45621593:G>A
ADCY1
NM_021116:c.639+6812G>A
INTRON1
Unknown significance
rs530675052
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
763173
chr7:45621607:A>T
ADCY1
NM_021116:c.639+6826A>T
INTRON1
Unknown significance
rs780640094
This variant is a VUS because it does not have enough information.
763174
chr7:45621618:C>T
ADCY1
NM_021116:c.639+6837C>T
INTRON1
Unknown significance
rs573546503
This variant is a VUS because it does not have enough information.
763175
chr7:45621622:CT>-
ADCY1
NM_021116:c.639+6841_639+6842delCT
INTRON1
Unknown significance
rs202181571
This variant is a VUS because it does not have enough information.
763176
chr7:45621624:CA>-
ADCY1
NM_021116:c.639+6843_639+6844delCA
INTRON1
Benign
rs141367514
This variant contains a MAF in at least one population that meets or exceeds our maximum cutoff of 0.005.