Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
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
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 187
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 118
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 106
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs11615 0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs4938723 0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs1051740 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs351855 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 55
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 55
rs2070744 0.608 0.680 7 150992991 intron variant C/T snv 0.70 53
rs20541 0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 47
rs10889677 0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
rs920778 0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs1800624 0.658 0.480 6 32184610 upstream gene variant A/G;T snv 33
rs145204276 0.658 0.320 1 173868254 splice donor variant CAAGG/- delins 8.8E-02 31
rs2071559
KDR
0.667 0.680 4 55126199 upstream gene variant A/G snv 0.53 26