Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs693 0.708 0.440 2 21009323 synonymous variant G/A snv 0.39 0.38 24
rs708272 0.708 0.440 16 56962376 intron variant G/A snv 0.42 0.38 24
rs1800961 0.851 0.160 20 44413724 missense variant C/T snv 3.1E-02 2.5E-02 21