Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs104894229 0.564 0.600 11 534289 missense variant C/A;G;T snv 73
rs104894228 0.605 0.560 11 534286 missense variant C/A;G;T snv 48