Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801157 0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16 46
rs2057482 0.701 0.440 14 61747130 3 prime UTR variant T/C snv 0.84 0.80 21
rs2735383 0.708 0.360 8 89935041 3 prime UTR variant C/G snv 0.31 18
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs5275 0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
rs568408 0.649 0.600 3 159995680 3 prime UTR variant G/A snv 0.16 29
rs712 0.677 0.360 12 25209618 3 prime UTR variant A/C snv 0.46 24
rs873601 0.677 0.360 13 102875987 3 prime UTR variant G/A snv 0.59 25
rs145204276 0.658 0.320 1 173868254 splice donor variant CAAGG/- delins 8.8E-02 31
rs132770 0.752 0.320 22 41621260 5 prime UTR variant A/G snv 0.83 14
rs1800734 0.653 0.400 3 36993455 5 prime UTR variant G/A snv 0.22 30
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
rs2070874
IL4
0.672 0.560 5 132674018 5 prime UTR variant C/T snv 0.28 0.28 27
rs2249825 0.695 0.440 13 30463766 5 prime UTR variant G/A;C;T snv 23
rs6505162 0.695 0.320 17 30117165 5 prime UTR variant A/C;T snv 0.50; 3.1E-05 25
rs751402 0.724 0.360 13 102845848 5 prime UTR variant A/G snv 0.76 15
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1128503 0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs11615 0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs199613843 0.807 0.160 19 43551609 synonymous variant C/T snv 4.0E-06 7.0E-06 6
rs2307181 0.851 0.120 19 43544170 synonymous variant G/A;C snv 6.1E-05 4
rs2736098 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 48
rs709816
NBN
0.752 0.320 8 89955483 synonymous variant A/G snv 0.47 0.51 10
rs10877887 0.701 0.440 12 62603400 non coding transcript exon variant T/C snv 0.42 18