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
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 34
rs72928038 0.695 0.360 6 90267049 intron variant G/A snv 0.11 19
rs11168249 0.807 0.120 12 47814585 intron variant T/C snv 0.50 8