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
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs727503094 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 41
rs2273535 0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 38
rs1273593548 0.716 0.160 7 106867593 missense variant T/G snv 8.4E-06 19
rs375874539 0.732 0.320 17 7674237 missense variant G/A;C snv 15