Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs2074755 0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02 20
rs11065987 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 17
rs9895661 0.882 0.200 17 61379228 non coding transcript exon variant C/T snv 0.69 10
rs9472135 0.925 0.120 6 43842065 intron variant T/A;C;G snv 9
rs11072566 0.925 0.120 15 76001630 intron variant A/G snv 0.45 5