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: rs1057518879
rs1057518879
19 0.776 0.280 1 11965571 stop gained G/A snv 0.700 0
dbSNP: rs1057518951
rs1057518951
5 0.827 0.160 6 156829296 stop gained C/T snv 0.700 0
dbSNP: rs1251778848
rs1251778848
11 0.790 0.400 12 49039277 stop gained G/A snv 0.700 0
dbSNP: rs1400419650
rs1400419650
38 0.708 0.320 14 92005938 stop gained C/A;T snv 4.0E-06 1.4E-05 0.700 0
dbSNP: rs35135520
rs35135520
12 0.827 0.200 19 39480879 stop gained C/A;G;T snv 3.1E-03; 4.6E-06 0.700 0
dbSNP: rs387906692
rs387906692
8 0.752 0.480 17 68530405 stop gained C/T snv 0.700 0
dbSNP: rs587782993
rs587782993
6 0.882 0.080 5 140114737 stop gained C/T snv 0.700 0
dbSNP: rs587782996
rs587782996
5 0.925 0.080 5 140114544 stop gained C/G;T snv 9.0E-06 0.700 0
dbSNP: rs587782997
rs587782997
5 0.925 0.080 5 140114964 stop gained C/G snv 0.700 0
dbSNP: rs770703007
rs770703007
8 0.851 0.120 16 1706450 stop gained C/G;T snv 4.0E-06 0.700 0
dbSNP: rs776019250
rs776019250
12 0.827 0.200 19 39482885 stop gained G/C;T snv 4.0E-06 0.700 0
dbSNP: rs912001256
rs912001256
17 0.851 0.240 17 63947062 stop gained G/A snv 0.700 0
dbSNP: rs121908557
rs121908557
19 0.752 0.280 17 63957514 missense variant C/T snv 8.2E-06 1.4E-05 0.700 1.000 2 2004 2008
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: rs1009298200
rs1009298200
34 0.742 0.400 16 5079077 missense variant C/G;T snv 7.0E-06 0.700 0
dbSNP: rs1057519389
rs1057519389
46 0.695 0.400 10 129957324 missense variant C/A;G;T snv 0.700 0
dbSNP: rs12720458
rs12720458
20 0.716 0.240 11 2585264 missense variant A/G snv 4.0E-05 1.4E-05 0.700 0
dbSNP: rs1421405659
rs1421405659
13 0.851 0.360 12 101642529 missense variant T/C;G snv 0.700 0
dbSNP: rs1555452127
rs1555452127
34 0.742 0.400 16 5079078 missense variant T/C snv 0.700 0
dbSNP: rs1563221666
rs1563221666
14 0.882 0.120 8 22162694 missense variant C/T snv 0.700 0
dbSNP: rs587777446
rs587777446
10 0.807 0.200 2 162273913 missense variant C/T snv 4.0E-06 0.700 0
dbSNP: rs587782994
rs587782994
6 0.882 0.080 5 140114470 missense variant A/G snv 0.700 0
dbSNP: rs587782995
rs587782995
42 0.708 0.360 5 140114480 missense variant T/C snv 0.700 0
dbSNP: rs587782998
rs587782998
5 0.882 0.080 5 140114651 missense variant T/A snv 0.700 0
dbSNP: rs587782999
rs587782999
6 0.882 0.080 5 140114446 missense variant G/A;C snv 0.700 0