Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11209026 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
rs1137100 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39
rs11465804 0.752 0.320 1 67236843 intron variant T/G snv 4.4E-02 5.4E-02 10
rs11584340 0.827 0.200 1 152313454 missense variant G/A snv 0.27 0.19 5
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
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
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs3021097 0.752 0.440 1 206773289 5 prime UTR variant A/G snv 10
rs4129267 0.807 0.200 1 154453788 intron variant C/G;T snv 13
rs4845604 0.776 0.200 1 151829204 intron variant G/A;C;T snv 10
rs5063 0.763 0.280 1 11847591 missense variant C/T snv 5.6E-02 5.3E-02 12
rs61816761 0.658 0.640 1 152313385 stop gained G/A;T snv 9.4E-03; 8.0E-06 43
rs1990760 0.672 0.480 2 162267541 missense variant C/T snv 0.50 0.45 33
rs549858786 0.790 0.320 2 112836807 5 prime UTR variant T/A snv 10
rs3197999 0.732 0.280 3 49684099 missense variant G/A snv 0.26 0.27 16
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs4696480 0.716 0.400 4 153685974 intron variant T/A snv 0.45 19
rs10036748 0.752 0.360 5 151078585 intron variant C/A;T snv 11
rs1295685 0.790 0.160 5 132660753 3 prime UTR variant A/G snv 0.81 7
rs1800925 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 37
rs20541 0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193