Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12826786 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 26
rs13361189 0.752 0.240 5 150843825 upstream gene variant T/C snv 0.21 13
rs398652 0.752 0.240 14 56058851 intergenic variant G/A snv 0.24 10
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs17655 0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs3212986 0.620 0.400 19 45409478 stop gained C/A;G;T snv 0.29; 4.3E-06; 4.3E-06 42
rs621559 0.827 0.080 1 43179740 intron variant G/A snv 0.18 5
rs4073 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35
rs11615 0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs2298881 0.653 0.400 19 45423658 intron variant C/A;T snv 25
rs1799793 0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29 72
rs2276466 0.732 0.320 16 13949318 3 prime UTR variant C/A;G snv 15
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs920778 0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1870377
KDR
0.695 0.520 4 55106807 missense variant T/A snv 0.22 0.20 25
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs1353702185 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79
rs773919809 0.763 0.200 10 129766957 missense variant C/T snv 2.0E-05 13