Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11137037 0.851 0.200 8 6538661 intron variant A/C snv 0.40 4
rs12674822 0.851 0.200 8 6531695 intron variant T/G snv 0.49 4
rs1412125 0.724 0.360 13 30467458 intron variant C/G;T snv 17
rs1535045 0.742 0.360 20 46119460 intron variant C/A;G;T snv 12
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs2075786 0.790 0.360 5 1266195 intron variant A/G snv 0.55 8
rs2281089 0.851 0.200 22 37136132 intron variant A/G snv 0.17 4
rs2395185 0.724 0.360 6 32465390 intron variant G/T snv 0.29 17
rs2847297 0.827 0.200 18 12797695 intron variant A/G snv 0.40 5
rs3117582 0.716 0.440 6 31652743 intron variant T/G snv 7.1E-02 14
rs3817963 0.776 0.360 6 32400310 intron variant T/C snv 0.25 8
rs767649 0.695 0.480 21 25572410 intron variant T/A snv 7.5E-02 18
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs791588 0.851 0.200 10 6047379 intron variant G/T snv 0.40 4
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs969129 0.851 0.200 5 35861166 intron variant T/A;G snv 4
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs11543848 0.790 0.240 7 55161562 missense variant G/A;C;T snv 7
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1222213359 0.574 0.720 6 43770966 missense variant G/A snv 62
rs1353702185 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79