Source: CURATED ×
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1208636573
rs1208636573
15 0.807 0.120 1 155612098 stop gained C/G;T snv 4.0E-06; 4.0E-06 0.700 0
dbSNP: rs201128942
rs201128942
5 0.851 0.120 6 85547112 stop gained C/A;T snv 2.4E-05 4.2E-05 0.700 0
dbSNP: rs774277300
rs774277300
17 0.742 0.360 11 94447276 stop gained G/A;C;T snv 2.8E-05; 4.0E-05; 4.0E-06 0.700 0
dbSNP: rs866294686
rs866294686
43 0.683 0.480 10 102657073 stop gained C/A;T snv 0.700 0
dbSNP: rs863223953
rs863223953
10 0.776 0.240 12 32731362 missense variant C/T snv 0.700 1.000 2 2016 2016
dbSNP: rs63750687
rs63750687
30 0.752 0.200 14 73217137 missense variant C/A;G;T snv 0.700 1.000 1 2014 2014
dbSNP: rs672601368
rs672601368
10 0.827 0.160 2 240785062 missense variant C/G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs752298579
rs752298579
48 0.701 0.480 22 20061538 missense variant G/A snv 1.4E-04 7.0E-06 0.700 1.000 1 2016 2016
dbSNP: rs779027563
rs779027563
58 0.677 0.360 17 42687838 missense variant G/C snv 4.0E-06 7.0E-06 0.700 1.000 1 2017 2017
dbSNP: rs1057519429
rs1057519429
14 0.807 0.240 19 13235666 missense variant C/G;T snv 0.700 0
dbSNP: rs1114167296
rs1114167296
6 0.827 0.160 X 34656995 missense variant C/G snv 0.700 0
dbSNP: rs139632595
rs139632595
19 0.807 0.160 4 121801465 missense variant T/C snv 6.0E-05 2.5E-04 0.700 0
dbSNP: rs1554107200
rs1554107200
4 0.851 0.120 5 140679127 missense variant C/A snv 0.700 0
dbSNP: rs1555570110
rs1555570110
9 0.827 0.240 17 7586766 missense variant A/C snv 0.700 0
dbSNP: rs1555745467
rs1555745467
23 0.752 0.240 19 13262771 missense variant C/A snv 0.700 0
dbSNP: rs28934907
rs28934907
29 0.732 0.320 X 154032268 missense variant G/A;C snv 0.700 0
dbSNP: rs387906799
rs387906799
17 0.742 0.200 2 240788118 missense variant G/A snv 0.700 0
dbSNP: rs587777721
rs587777721
4 0.925 0.160 12 51806336 missense variant G/A snv 0.700 0
dbSNP: rs622288
rs622288
15 0.807 0.120 1 155612848 missense variant C/T snv 3.6E-05 4.2E-05 0.700 0
dbSNP: rs672601362
rs672601362
7 0.851 0.080 2 240789246 missense variant G/A snv 0.700 0
dbSNP: rs672601363
rs672601363
6 0.851 0.080 2 240788109 missense variant C/T snv 0.700 0
dbSNP: rs672601367
rs672601367
7 0.851 0.080 2 240785066 missense variant T/G snv 0.700 0
dbSNP: rs672601369
rs672601369
10 0.790 0.120 2 240783780 missense variant C/T snv 0.700 0
dbSNP: rs672601370
rs672601370
13 0.790 0.160 2 240775863 missense variant G/A snv 0.700 0
dbSNP: rs750331613
rs750331613
5 0.882 0.040 4 93515346 missense variant C/T snv 4.8E-05 2.1E-05 0.700 0