Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1046282 0.776 0.160 19 45407414 3 prime UTR variant A/G snv 0.30 10
rs1058808 0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52 27
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 484
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs11540652 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 20
rs121434568 0.568 0.560 7 55191822 missense variant T/A;G snv 73
rs121434569 0.581 0.520 7 55181378 missense variant C/T snv 2.8E-05 5.6E-05 70
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 135
rs121917887 0.790 0.120 17 51161744 missense variant A/G snv 6.0E-05 7.0E-05 10
rs12918952 0.851 0.120 16 78386878 missense variant G/A;C;T snv 7
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs1329032366 0.882 0.080 4 94654530 missense variant A/G snv 4.0E-06 5
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 106
rs1800624 0.658 0.480 6 32184610 upstream gene variant A/G;T snv 33
rs1800625 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 35
rs1801131 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 92
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 169
rs1801270 0.689 0.400 6 36684194 missense variant C/A;T snv 0.15; 4.4E-05 22
rs1982073 0.649 0.640 19 41353016 missense variant G/A;C snv 32
rs2066853
AHR
0.653 0.600 7 17339486 missense variant G/A snv 0.15 0.22 34
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 75
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs2279744 0.605 0.640 12 68808800 intron variant T/G snv 0.31 47
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 47
rs28934578 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 36