Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2042329 0.882 0.120 5 64771925 intron variant T/C;G snv 3
rs2074647 0.882 0.120 14 72562470 missense variant G/A snv 9.0E-02 0.10 3
rs2228104
POR
0.882 0.120 7 75985635 synonymous variant T/A;C snv 4.5E-06; 0.92 3
rs2664139 0.882 0.120 15 39580382 upstream gene variant T/C snv 0.41 3
rs3213255 0.882 0.120 19 43573355 intron variant G/A snv 0.60 3
rs3213356 0.882 0.120 19 43554087 intron variant C/T snv 0.60 3
rs3219493 0.882 0.120 1 45330597 intron variant G/C snv 0.92 0.93 3
rs377062126 0.882 0.120 12 104319543 missense variant G/A snv 2.1E-05 3.5E-05 3
rs4969054 0.882 0.120 17 73016334 intron variant G/C snv 0.73 3
rs4986826
AHR
0.882 0.120 7 17339533 missense variant G/A snv 7.8E-03 2.2E-02 3
rs62185668 0.925 0.120 20 10981287 intron variant C/A snv 0.19 3
rs6464268 0.882 0.120 7 152684065 intergenic variant A/G snv 0.23 3
rs715021 0.882 0.120 2 221196620 intergenic variant C/G snv 0.26 3
rs72552316 0.882 0.120 X 12889591 3 prime UTR variant T/C snv 3
rs7257330 0.882 0.120 19 29810916 upstream gene variant G/A snv 0.30 3
rs7431 0.882 0.120 8 22540949 3 prime UTR variant G/A snv 0.56 3
rs758057623 0.882 0.120 11 67584520 missense variant G/A snv 3
rs771866347 0.882 0.120 3 49358109 missense variant G/A snv 4.1E-06 3
rs7832529 0.882 0.120 8 42449295 intron variant T/C snv 0.24 3
rs8041357 0.882 0.120 15 74577097 intron variant T/C snv 6.6E-02 3
rs8102137 0.882 0.120 19 29805946 regulatory region variant T/C snv 0.24 3
rs8444 0.882 0.120 1 150966095 3 prime UTR variant G/A snv 0.35 3
rs861531 0.882 0.120 14 103706470 3 prime UTR variant C/A snv 0.32 3
rs921142 0.882 0.120 8 41311757 upstream gene variant T/C snv 0.31 3
rs9624880 0.882 0.120 22 25588025 intron variant C/T snv 3