Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5743708 0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 97
rs25490 0.851 0.120 19 43552189 missense variant T/C snv 7.2E-03 2.6E-02 4
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 230
rs9288516 0.827 0.120 2 216188541 intron variant T/A snv 5.0E-02 6
rs1138272 0.611 0.600 11 67586108 missense variant C/T snv 5.9E-02 5.5E-02 42
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs3025039 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs7963551 0.807 0.160 12 912349 3 prime UTR variant T/G snv 0.13 7
rs621559 0.827 0.080 1 43179740 intron variant G/A snv 0.18 5
rs1870377
KDR
0.695 0.520 4 55106807 missense variant T/A snv 0.22 0.20 25
rs2736098 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 46
rs398652 0.752 0.240 14 56058851 intergenic variant G/A snv 0.24 9
rs1805377 0.689 0.480 5 83353124 splice acceptor variant G/A snv 0.23 0.25 19
rs3212227 0.566 0.840 5 159315942 3 prime UTR variant T/G snv 0.26 65
rs1801131 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 92
rs2070874
IL4
0.672 0.560 5 132674018 5 prime UTR variant C/T snv 0.28 0.28 27
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 103
rs1805794
NBN
0.605 0.600 8 89978251 missense variant C/G snv 0.35 0.31 41
rs4938723 0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 110
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 187
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 153
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35