Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1293762 1.000 0.080 12 112993031 intron variant T/G snv 0.67 1
rs12952093 1.000 0.080 17 78367559 intron variant A/C;T snv 1
rs2779180 1.000 0.080 19 4841139 intron variant A/G snv 0.37 1
rs965469 1.000 0.080 20 3400902 intron variant T/C snv 0.20 1
rs9461776 0.763 0.240 6 32607958 intergenic variant A/G snv 8.8E-02 11
rs10776934 1.000 0.080 9 135137855 regulatory region variant T/G snv 0.74 1
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs5743708 0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs738409 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs3775291 0.602 0.640 4 186082920 missense variant C/G;T snv 1.2E-04; 0.28 51
rs58542926 0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42
rs1127354 0.667 0.400 20 3213196 missense variant C/A;G snv 7.5E-02 26
rs6897932 0.683 0.560 5 35874473 missense variant C/T snv 0.23 0.21 25
rs12075 0.724 0.240 1 159205564 missense variant G/A snv 0.51 0.66 22
rs641738 0.689 0.320 19 54173068 missense variant T/A;C;G snv 22
rs2287622 0.724 0.240 2 168973818 missense variant A/C;G;T snv 0.57 16
rs3747517 0.732 0.360 2 162272314 missense variant T/C snv 0.68 0.68 13
rs5743704 0.763 0.240 4 153704799 missense variant C/A snv 2.8E-02 2.8E-02 9
rs758564400
REN
0.925 0.120 1 204156683 missense variant A/G snv 4.0E-06 5
rs8103142 0.882 0.120 19 39244466 missense variant T/C snv 0.29 0.40 4