Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2981582 0.695 0.360 10 121592803 intron variant A/G snv 0.58 21
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs61764370 0.662 0.320 12 25207290 3 prime UTR variant A/C snv 6.2E-02 29
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 62
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs920778 0.633 0.480 12 53966448 intron variant G/A snv 0.57 36