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 61
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 55
rs12454712 0.925 0.120 18 63178651 intron variant T/A;C snv 7
rs11048456 1.000 0.080 12 26310149 intron variant C/T snv 0.62 6
rs13389219 1.000 0.080 2 164672366 intron variant C/T snv 0.47 5
rs702634 1.000 0.080 5 53975590 intron variant G/A snv 0.72 3