Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
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
rs20417 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 57
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs5275 0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
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
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
rs13361189 0.752 0.240 5 150843825 upstream gene variant T/C snv 0.21 13
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs3025039 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs833061 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 42
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs1799931 0.742 0.320 8 18400860 missense variant G/A snv 5.8E-02 3.9E-02 14
rs1805794
NBN
0.605 0.600 8 89978251 missense variant C/G snv 0.35 0.31 41
rs12917 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 45