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-06 135
rs121913530 0.583 0.640 12 25245351 missense variant C/A;G;T snv 55
rs712 0.677 0.360 12 25209618 3 prime UTR variant A/C snv 0.46 24
rs121913240 0.672 0.440 12 25227342 missense variant T/A;C;G snv 19
rs17851045 0.672 0.400 12 25227341 missense variant T/A;G snv 4.0E-06 12
rs104894360 0.724 0.560 12 25209904 missense variant T/A;C snv 2