Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs63751273 0.645 0.280 17 46010389 missense variant C/T snv 42
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs9296158 0.763 0.080 6 35599305 intron variant A/G snv 0.65 16
rs9340799 0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs9470080 0.827 0.080 6 35678658 intron variant T/A;C snv 13