Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs3816873 0.790 0.200 4 99583507 missense variant T/C snv 0.25 0.26 9
rs33957861 0.882 0.160 10 67887218 intron variant C/T snv 0.11 3
rs11599176 0.925 0.080 10 67894017 intron variant A/G snv 0.11 2
rs35689145 1.000 0.080 10 67900009 intron variant G/A;C snv 1