Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs1800796 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs2066853
AHR
0.653 0.600 7 17339486 missense variant G/A snv 0.15 0.22 34
rs2606345 0.732 0.360 15 74724835 intron variant C/A snv 0.46 16
rs3774934 0.851 0.080 4 102506319 intron variant A/C;G;T snv 4