Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12674822 0.851 0.200 8 6531695 intron variant T/G snv 0.49 4
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1801131 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs3117582 0.716 0.440 6 31652743 intron variant T/G snv 7.1E-02 14
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1883832 0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs3817963 0.776 0.360 6 32400310 intron variant T/C snv 0.25 8
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs969129 0.851 0.200 5 35861166 intron variant T/A;G snv 4
rs767649 0.695 0.480 21 25572410 intron variant T/A snv 7.5E-02 18
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs2395185 0.724 0.360 6 32465390 intron variant G/T snv 0.29 17
rs2929973 0.851 0.200 8 133230265 3 prime UTR variant G/T snv 0.85 5
rs791588 0.851 0.200 10 6047379 intron variant G/T snv 0.40 4
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs2231142 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 56
rs1800796 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs11543848 0.790 0.240 7 55161562 missense variant G/A;C;T snv 7
rs2249825 0.695 0.440 13 30463766 5 prime UTR variant G/A;C;T snv 23
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs1222213359 0.574 0.720 6 43770966 missense variant G/A snv 62
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs1799930 0.716 0.400 8 18400593 missense variant G/A snv 0.27 0.27 17