Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3743930 0.611 0.720 16 3254626 missense variant C/G;T snv 7.1E-02 43
rs909253 0.641 0.600 6 31572536 intron variant A/G;T snv 34
rs7044343 0.752 0.520 9 6254208 intron variant C/T snv 0.51 13
rs2187668 0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 20
rs1137100 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39
rs555743307 0.695 0.440 16 27342243 missense variant G/A;T snv 3.6E-05; 2.9E-04 20
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs187238 0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs1946518 0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs549908 0.752 0.440 11 112150193 synonymous variant T/A;G snv 4.2E-06; 0.29 10
rs2397084 0.716 0.480 6 52237046 missense variant T/C snv 6.7E-02 6.1E-02 14
rs763780 0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs3819024 0.701 0.560 6 52185988 upstream gene variant A/G snv 0.34 17
rs8193036 0.689 0.600 6 52185695 upstream gene variant C/T snv 0.72 21
rs20541 0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52
rs3212227 0.566 0.840 5 159315942 3 prime UTR variant T/G snv 0.26 65
rs2069718 0.742 0.320 12 68156382 intron variant A/G;T snv 0.50 14
rs2430561 0.590 0.760 12 68158742 intron variant T/A snv 0.36 50
rs2069705 0.695 0.440 12 68161231 intron variant G/A;C snv 19
rs1990760 0.672 0.480 2 162267541 missense variant C/T snv 0.50 0.45 33
rs1063320 0.752 0.360 6 29830972 3 prime UTR variant C/G;T snv 12