Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12979860 0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs738409 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs243865 0.600 0.640 16 55477894 intron variant C/T snv 0.19 48
rs3918242 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 54
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
rs10889677 0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
rs1137100 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39
rs58542926 0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42
rs1061622 0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 33
rs187084 0.641 0.480 3 52227015 intron variant A/G snv 0.38 36
rs28934571 0.645 0.360 17 7674216 missense variant C/A;G snv 31
rs1800730 0.649 0.480 6 26090957 missense variant A/T snv 1.0E-02 1.0E-02 32
rs4950928 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 33
rs4898 0.672 0.520 X 47585586 synonymous variant T/C snv 0.46 0.46 25
rs2227982 0.677 0.480 2 241851281 missense variant G/A snv 9.2E-02 4.3E-02 24
rs6897932 0.683 0.560 5 35874473 missense variant C/T snv 0.23 0.21 25
rs61750420 0.689 0.480 7 92501562 missense variant C/T snv 3.2E-04 3.5E-04 52
rs641738 0.689 0.320 19 54173068 missense variant T/A;C;G snv 22
rs1870377
KDR
0.695 0.520 4 55106807 missense variant T/A snv 0.22 0.20 25
rs6505162 0.695 0.320 17 30117165 5 prime UTR variant A/C;T snv 0.50; 3.1E-05 25
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23