Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs121434568 0.568 0.560 7 55191822 missense variant T/A;G snv 73
rs1057519847 0.570 0.560 7 55191821 missense variant CT/AG mnv 72
rs1057519848 0.570 0.560 7 55191822 missense variant TG/GT mnv 72
rs11554290 0.583 0.600 1 114713908 missense variant T/A;C;G snv 59
rs2070744 0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs3918242 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 54
rs2279744 0.605 0.640 12 68808800 intron variant T/G snv 0.31 48
rs3761548 0.620 0.680 X 49261784 intron variant G/A;T snv 42
rs1800625 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs1057519695 0.641 0.520 1 114713907 missense variant TT/CA;CC mnv 35
rs1800624 0.658 0.480 6 32184610 upstream gene variant A/G;T snv 33
rs4950928 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 33
rs1982073 0.649 0.640 19 41353016 missense variant G/A;C snv 32
rs1057519834 0.658 0.480 1 114713908 missense variant TG/CT mnv 31
rs145204276 0.658 0.320 1 173868254 splice donor variant CAAGG/- delins 8.8E-02 31
rs531564 0.672 0.480 8 9903189 non coding transcript exon variant G/C snv 0.14 27
rs2071559
KDR
0.667 0.680 4 55126199 upstream gene variant A/G snv 0.53 26
rs121909218 0.672 0.360 10 87933145 missense variant G/A snv 25
rs4939827 0.708 0.160 18 48927093 intron variant T/A;C snv 25
rs121913412 0.724 0.280 3 41224633 missense variant A/C;G;T snv 19
rs937283 0.716 0.200 12 68808384 5 prime UTR variant A/G snv 0.37 19
rs3798577 0.742 0.320 6 152099995 3 prime UTR variant T/C snv 0.45 16
rs11568818 0.763 0.280 11 102530930 upstream gene variant T/A;C snv 15