Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1870377
KDR
0.695 0.520 4 55106807 missense variant T/A snv 0.22 0.20 25
rs20541 0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 47
rs2307191 0.827 0.120 19 43553616 missense variant G/A snv 1.2E-03 4.8E-03 5
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 114
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs25489 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78
rs25490 0.851 0.120 19 43552189 missense variant T/C snv 7.2E-03 2.6E-02 4
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs5743708 0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 97
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 153
rs72554204 0.827 0.120 19 43546062 missense variant C/T snv 1.2E-04 1.3E-04 5
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 103
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs1800925 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 37
rs20417 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 57
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
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
rs2736098 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 46
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 107
rs2070874
IL4
0.672 0.560 5 132674018 5 prime UTR variant C/T snv 0.28 0.28 27
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 73
rs3025039 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs3212227 0.566 0.840 5 159315942 3 prime UTR variant T/G snv 0.26 65