Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3764650 0.790 0.200 19 1046521 intron variant T/G snv 0.14 2
rs115550680 1.000 0.080 19 1050421 intron variant A/G snv 1.7E-02 1
rs3752246 1.000 0.080 19 1056493 missense variant G/C;T snv 0.84; 4.1E-06 1
rs4147929 0.882 0.120 19 1063444 intron variant A/C;G snv 1