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 52
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 36
rs121913482 0.630 0.680 4 1801837 missense variant C/T snv 35
rs104894228 0.605 0.560 11 534286 missense variant C/A;G;T snv 30
rs11554290 0.583 0.600 1 114713908 missense variant T/A;C;G snv 25
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 19
rs121913237 0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 12