Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2736098 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 46
rs833061 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 42
rs11615 0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs1799793 0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29 72
rs2071559
KDR
0.667 0.680 4 55126199 upstream gene variant A/G snv 0.53 26
rs4938723 0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 103
rs1353702185 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79
rs20541 0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 47
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 114
rs25489 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78
rs3025039 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 110
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 213
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 107
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs5743708 0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 97
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1801131 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 92
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101