Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs2293607 0.807 0.200 3 169764547 non coding transcript exon variant T/A;C snv 6
rs1048943 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs8034191 0.695 0.440 15 78513681 intron variant T/C snv 0.27 24
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306