Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs187238 0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs25531 0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72