Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs11209026 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
rs5029939 0.701 0.440 6 137874586 intron variant C/G snv 0.13 19
rs8192284 0.724 0.720 1 154454494 missense variant A/C;T snv 19
rs11805303 0.827 0.240 1 67209833 intron variant C/T snv 0.30 6
rs6933404 0.925 0.280 6 137638098 intergenic variant T/C snv 0.16 5