Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1613662 0.851 0.120 19 55025227 missense variant G/A snv 0.85 0.83 8
rs10886430 10 119250744 intron variant A/G snv 8.8E-02 3
rs12445050 16 81837364 intron variant C/T snv 9.6E-02 3