Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs2304256 0.732 0.360 19 10364976 missense variant C/A snv 0.27 0.23 13
rs12720356 0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06 12
rs12720270 0.851 0.240 19 10365084 intron variant G/A snv 0.21 0.16 4
rs280500 0.882 0.200 19 10379726 5 prime UTR variant A/G snv 0.20 3