Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1016604233 1.000 0.080 7 139911241 missense variant C/T snv 8.0E-06 2.1E-05 1
rs1033602309 1.000 0.080 X 9937279 missense variant G/C snv 1
rs1034429230 1.000 0.080 1 212365260 missense variant C/G snv 1.4E-05 1
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 4
rs104894097 0.807 0.240 9 21974757 missense variant C/A;G;T snv 1.7E-05; 1.3E-05 1
rs1057519927 0.716 0.240 3 179218295 missense variant A/C;G;T snv 1
rs1057519981 0.689 0.440 17 7674251 missense variant A/C;G;T snv 1
rs1060502347 1.000 0.080 17 43091902 missense variant T/C snv 4.0E-06 1
rs111265129 1.000 0.080 10 16851333 missense variant T/C snv 3.3E-03 1.3E-02 1
rs111299050 1.000 0.080 11 31370815 missense variant A/G snv 4.3E-04 2.2E-03 1
rs111367604 1.000 0.080 2 214728927 missense variant C/A;G;T snv 8.0E-06 1
rs112523432 1.000 0.080 1 214384776 missense variant T/C;G snv 4.0E-06; 5.9E-03 1
rs112973609 1.000 0.080 11 120118309 missense variant G/A snv 2.0E-05 1
rs113117391 1.000 0.080 8 52628128 missense variant G/A snv 2.2E-04 2.5E-04 1
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 1
rs113776284 1.000 0.080 2 227893863 missense variant C/T snv 3.6E-05 3.5E-05 1
rs11540652 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 1
rs11571747 1.000 0.080 13 32371035 missense variant A/C snv 1.1E-03 1.5E-03 1
rs11571769 1.000 0.080 13 32379413 missense variant G/A;T snv 9.5E-03 8.2E-03 1
rs116076204 1.000 0.080 18 45870626 missense variant G/A;C snv 7.1E-04; 1.2E-05 1
rs11643870 1.000 0.080 16 84318346 missense variant G/A snv 8.8E-03 8.4E-03 1
rs1165078436 1.000 0.080 1 31798459 missense variant G/A snv 4.0E-06 7.0E-06 1
rs1165723137
CRX
1.000 0.080 19 47839489 missense variant C/T snv 4.0E-06 1
rs1165948169 1.000 0.080 12 47798799 missense variant C/T snv 1
rs116967198 1.000 0.080 18 13681833 missense variant C/A;T snv 4.0E-06; 1.2E-05 1