Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs874945 0.732 0.240 12 53961667 upstream gene variant C/T snv 0.38 14
rs10811474 0.742 0.240 9 21114238 intergenic variant A/G snv 0.44 11
rs398652 0.752 0.240 14 56058851 intergenic variant G/A snv 0.24 10
rs1495741 0.827 0.240 8 18415371 regulatory region variant G/A snv 0.71 9
rs1109324 0.827 0.160 6 43762018 intergenic variant G/T snv 0.15 5
rs833052 0.827 0.160 6 43755598 intergenic variant A/C snv 0.88 5
rs1547651 0.851 0.200 6 43762907 regulatory region variant A/T snv 0.15 4
rs2505568 0.851 0.160 10 36522408 non coding transcript exon variant T/A snv 0.56 4
rs2764736 0.851 0.160 9 25067733 intergenic variant T/C snv 2.4E-02 4
rs710521 0.851 0.200 3 189928144 intergenic variant T/C snv 0.24 4
rs1014971 0.882 0.120 22 38936618 regulatory region variant C/T snv 0.55 3
rs10234749 0.882 0.120 7 152690784 regulatory region variant T/C;G snv 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
rs8102137 0.882 0.120 19 29805946 regulatory region variant T/C snv 0.24 3
rs921142 0.882 0.120 8 41311757 upstream gene variant T/C snv 0.31 3
rs1937920 0.925 0.120 10 5119763 downstream gene variant A/G snv 0.28 2
rs2066853
AHR
0.653 0.600 7 17339486 missense variant G/A snv 0.15 0.22 34
rs4986826
AHR
0.882 0.120 7 17339533 missense variant G/A snv 7.8E-03 2.2E-02 3
rs4957014
AHRR ; PDCD6
0.752 0.160 5 287899 intron variant T/G snv 0.74 11
rs12529
AKR1C3
0.776 0.280 10 5094459 missense variant C/G snv 0.50 0.45 10
rs121434592
AKT1
0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs3730358
AKT1
0.724 0.360 14 104780070 intron variant G/A;C snv 0.16; 4.0E-03 14