Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11556924 0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 21
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs7819412 0.827 0.120 8 11187652 intron variant G/A;T snv 6
rs3025039 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs231150 0.925 0.080 8 115408099 downstream gene variant A/T snv 0.55 2
rs11536889 0.658 0.560 9 117715853 3 prime UTR variant G/C snv 0.11 27
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs6882076 0.827 0.160 5 156963286 upstream gene variant T/C snv 0.56 9
rs1042579 0.732 0.240 20 23048087 missense variant G/A;T snv 0.19 16
rs147377392 0.763 0.120 20 23048144 missense variant A/G snv 1.0E-04 2.8E-04 11
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs1044925 0.827 0.120 1 179354603 3 prime UTR variant C/A;G snv 6
rs1764391 0.790 0.160 1 34795168 missense variant C/G;T snv 0.30 7
rs1122608 0.763 0.120 19 11052925 intron variant G/T snv 0.18 16
rs9797861 0.790 0.200 19 10632450 intron variant C/A;G;T snv 9
rs1051266 0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 41
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs1799889 0.649 0.600 7 101126430 upstream gene variant A/G snv 31
rs2228315 0.807 0.120 12 108624122 missense variant C/T snv 0.11 0.14 7
rs6131 0.851 0.200 1 169611647 missense variant C/T snv 0.20 0.22 4
rs6136 0.752 0.440 1 169594713 missense variant T/G snv 8.2E-02 7.5E-02 17
rs5361 0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 47
rs5888 0.752 0.200 12 124800202 synonymous variant A/G;T snv 0.59; 4.0E-06 11