Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11209026 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 5
rs2201841 0.716 0.440 1 67228519 intron variant A/G;T snv 4
rs10865331 0.827 0.120 2 62324337 intergenic variant A/G snv 0.57 3
rs12720356 0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06 2
rs9988642 0.882 0.080 1 67260421 downstream gene variant T/C snv 0.13 2