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
rs61764370 0.662 0.320 12 25207290 3 prime UTR variant A/C snv 6.2E-02 29
rs112445441 0.658 0.400 12 25245347 missense variant C/A;G;T snv 24
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
rs121913238 0.732 0.240 12 25227343 missense variant G/C;T snv 14
rs121913527 0.807 0.320 12 25225628 missense variant C/A;G;T snv 6
rs1137188 1.000 0.080 12 25206418 3 prime UTR variant G/A snv 0.49 2
rs397517040 0.925 0.120 12 25245346 synonymous variant G/A;T snv 4.0E-06 1
rs7960917 1.000 0.080 12 25208712 3 prime UTR variant T/C snv 0.18 1
rs8720 1.000 0.080 12 25206009 3 prime UTR variant T/C snv 0.49 1