Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs20417 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 57
rs20541 0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 47
rs2070874
IL4
0.672 0.560 5 132674018 5 prime UTR variant C/T snv 0.28 0.28 27
rs2071559
KDR
0.667 0.680 4 55126199 upstream gene variant A/G snv 0.53 26
rs2298881 0.653 0.400 19 45423658 intron variant C/A;T snv 25
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
rs2736098 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 46
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 73
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
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
rs3212986 0.620 0.400 19 45409478 stop gained C/A;G;T snv 0.29; 4.3E-06; 4.3E-06 42
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs398652 0.752 0.240 14 56058851 intergenic variant G/A snv 0.24 9
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35
rs4938723 0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs5275 0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
rs5743708 0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 97
rs621559 0.827 0.080 1 43179740 intron variant G/A snv 0.18 5
rs6489769 0.851 0.120 12 963799 intron variant C/A;T snv 4
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 153