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
rs121913530 0.583 0.640 12 25245351 missense variant C/A;G;T snv 63
rs11554290 0.583 0.600 1 114713908 missense variant T/A;C;G snv 59
rs121913237 0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 50
rs1057519695 0.641 0.520 1 114713907 missense variant TT/CA;CC mnv 35
rs1057519834 0.658 0.480 1 114713908 missense variant TG/CT mnv 31
rs121913250 0.683 0.440 1 114716127 missense variant C/A;G;T snv 25
rs121913240 0.672 0.440 12 25227342 missense variant T/A;C;G snv 24
rs6449182 0.807 0.160 4 15778830 intron variant C/G snv 0.22 6