Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs4073 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs11615 0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs20417 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 57
rs5275 0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
rs10069690 0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs17655 0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs20541 0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52
rs2736098 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 48
rs397517132 0.623 0.280 7 55191846 missense variant A/T snv 48
rs12917 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 45
rs1138272 0.611 0.600 11 67586108 missense variant C/T snv 5.9E-02 5.5E-02 42
rs118101777 0.614 0.280 15 90087472 missense variant C/T snv 2.0E-03 1.6E-03 42
rs3212986 0.620 0.400 19 45409478 stop gained C/A;G;T snv 0.29; 4.3E-06; 4.3E-06 42
rs833061 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 42
rs1805794
NBN
0.605 0.600 8 89978251 missense variant C/G snv 0.35 0.31 41
rs78378222 0.662 0.360 17 7668434 3 prime UTR variant T/G snv 8.3E-03 37
rs1444669684 0.658 0.480 9 21994285 missense variant C/A;T snv 36
rs920778 0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs2066853
AHR
0.653 0.600 7 17339486 missense variant G/A snv 0.15 0.22 34
rs2308321 0.653 0.480 10 129766800 missense variant A/G snv 9.3E-02 8.7E-02 29
rs2853676 0.667 0.560 5 1288432 intron variant T/A;C snv 29
rs4246215 0.677 0.320 11 61796827 3 prime UTR variant G/C;T snv 29
rs2070874
IL4
0.672 0.560 5 132674018 5 prime UTR variant C/T snv 0.28 0.28 27
rs12826786 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 26