Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs5743708 0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs1801275 0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36 58
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs1800925 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 37
rs2066853
AHR
0.653 0.600 7 17339486 missense variant G/A snv 0.15 0.22 34
rs35829419 0.689 0.560 1 247425556 missense variant C/A snv 3.9E-02 3.3E-02 23
rs555743307 0.695 0.440 16 27342243 missense variant G/A;T snv 3.6E-05; 2.9E-04 20
rs1893592 0.742 0.280 21 42434957 missense variant A/C;G snv 0.27; 8.0E-06 12
rs5029949 0.925 0.120 6 137876369 intron variant A/G snv 8.1E-02 2