Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs1042713 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs20541 0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52
rs2070874
IL4
0.672 0.560 5 132674018 5 prime UTR variant C/T snv 0.28 0.28 27
rs10767664 0.752 0.400 11 27704439 intron variant T/A snv 0.83 16
rs7216389 0.732 0.440 17 39913696 intron variant C/T snv 0.60 14
rs8065080 0.827 0.200 17 3577153 missense variant T/C snv 0.37 0.32 11
rs8076131 0.790 0.200 17 39924659 intron variant G/A;C snv 11
rs121912633 0.790 0.240 12 109792396 missense variant C/A;T snv 4.0E-06 10
rs1342326 0.790 0.360 9 6190076 intergenic variant A/C snv 0.21 9
rs6967330 0.827 0.120 7 106018005 missense variant G/A snv 0.19 0.21 8
rs528557 0.827 0.120 20 3671095 synonymous variant C/A;G snv 4.7E-06; 0.29 6
rs3742030 0.925 0.080 12 109814742 missense variant G/A;C snv 3.7E-02 4
rs2569191 1.000 0.080 5 140634318 upstream gene variant C/A;T snv 2