Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801131 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs1353702185 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79
rs25489 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78
rs1799793 0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29 72
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs3212227 0.566 0.840 5 159315942 3 prime UTR variant T/G snv 0.26 65
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
rs3025039 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs4938723 0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs1801275 0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36 58
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
rs121913499 0.605 0.520 2 208248389 missense variant G/A;C;T snv 51
rs397517132 0.623 0.280 7 55191846 missense variant A/T snv 48
rs2736098 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 48
rs12917 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 45
rs3212986 0.620 0.400 19 45409478 stop gained C/A;G;T snv 0.29; 4.3E-06; 4.3E-06 42
rs1049353 0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42