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
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs121913237 0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 50
rs727503094 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 41