Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs104894226 0.658 0.560 11 534285 missense variant C/A;G;T snv 29