Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs1535 0.752 0.240 11 61830500 intron variant A/G snv 0.31 18
rs4246215 0.677 0.320 11 61796827 3 prime UTR variant G/C;T snv 13
rs7495132 0.790 0.080 15 90629669 intron variant C/T snv 0.12 10