Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs61839660 0.776 0.280 10 6052734 intron variant C/T snv 5.7E-02 9
rs20541 0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 4