Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17006625 0.925 0.080 3 20119604 missense variant A/C;G snv 4.0E-06; 3.3E-02 3
rs25490 0.851 0.120 19 43552189 missense variant T/C snv 7.2E-03 2.6E-02 4
rs6489769 0.851 0.120 12 963799 intron variant C/A;T snv 4
rs2307191 0.827 0.120 19 43553616 missense variant G/A snv 1.2E-03 4.8E-03 5
rs621559 0.827 0.080 1 43179740 intron variant G/A snv 0.18 5
rs72554204 0.827 0.120 19 43546062 missense variant C/T snv 1.2E-04 1.3E-04 5
rs199613843 0.807 0.160 19 43551609 synonymous variant C/T snv 4.0E-06 7.0E-06 6
rs9288516 0.827 0.120 2 216188541 intron variant T/A snv 5.0E-02 6
rs148611340 0.790 0.120 19 43543621 missense variant G/A;C snv 4.0E-06; 1.2E-05 7
rs7963551 0.807 0.160 12 912349 3 prime UTR variant T/G snv 0.13 7
rs1214285376 0.776 0.200 19 43543490 missense variant G/T snv 4.0E-06 8
rs398652 0.752 0.240 14 56058851 intergenic variant G/A snv 0.24 10
rs1805377 0.689 0.480 5 83353124 splice acceptor variant G/A snv 0.23 0.25 19
rs1870377
KDR
0.695 0.520 4 55106807 missense variant T/A snv 0.22 0.20 25
rs2298881 0.653 0.400 19 45423658 intron variant C/A;T snv 25
rs121912660 0.683 0.240 17 7673781 missense variant C/A;G;T snv 26
rs2071559
KDR
0.667 0.680 4 55126199 upstream gene variant A/G snv 0.53 26
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
rs920778 0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs1800925 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 37
rs28934575 0.641 0.400 17 7674230 missense variant C/A;G;T snv 37
rs1805794
NBN
0.605 0.600 8 89978251 missense variant C/G snv 0.35 0.31 41
rs1138272 0.611 0.600 11 67586108 missense variant C/T snv 5.9E-02 5.5E-02 42
rs3212986 0.620 0.400 19 45409478 stop gained C/A;G;T snv 0.29; 4.3E-06; 4.3E-06 42