Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2256175 1.000 6 31412672 intron variant C/T snv 0.55 5
rs2596542 0.724 0.200 6 31398818 upstream gene variant C/T snv 0.41 5
rs1051794 0.925 0.120 6 31411332 missense variant G/A snv 0.34 0.35 4
rs6910087 1.000 6 31409270 intron variant C/T snv 0.20 4
rs9266825 1.000 6 31415105 3 prime UTR variant C/A;T snv 0.31; 8.1E-06 4