Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs9303277 0.790 0.240 17 39820216 intron variant C/T snv 0.52 9
rs422112 1.000 0.080 17 45650771 non coding transcript exon variant G/A snv 0.14 3
rs5757611 1.000 0.080 22 39312352 downstream gene variant C/T snv 0.19 2