Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1214285376 0.776 0.200 19 43543490 missense variant G/T snv 4.0E-06 8
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs1273593548 0.716 0.160 7 106867593 missense variant T/G snv 8.4E-06 19
rs12917 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 45
rs1353702185 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79
rs1444669684 0.658 0.480 9 21994285 missense variant C/A;T snv 36
rs148611340 0.790 0.120 19 43543621 missense variant G/A;C snv 4.0E-06; 1.2E-05 7
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs17655 0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs1799793 0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29 72
rs1800067 0.716 0.320 16 13935176 missense variant G/A snv 5.6E-02 5.3E-02 17
rs1800371 0.742 0.240 17 7676230 missense variant G/A;T snv 1.2E-03 15
rs1801131 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs1805388 0.790 0.120 13 108211243 missense variant G/A snv 0.18 0.16 11
rs1805794
NBN
0.605 0.600 8 89978251 missense variant C/G snv 0.35 0.31 41
rs20541 0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52
rs2066853
AHR
0.653 0.600 7 17339486 missense variant G/A snv 0.15 0.22 34
rs2307191 0.827 0.120 19 43553616 missense variant G/A snv 1.2E-03 4.8E-03 5
rs2308321 0.653 0.480 10 129766800 missense variant A/G snv 9.3E-02 8.7E-02 29
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs25489 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306