Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1048943 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs4646903 0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18 36
rs2606345 0.732 0.360 15 74724835 intron variant C/A snv 0.46 16