Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
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
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs17655 0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
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 0.34 111
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs12826786 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 26
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 0.42 157
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
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
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs11615 0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs920778 0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205