Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1051740 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs10889677 0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs16893344 0.807 0.160 8 133194036 intron variant C/T snv 0.29 6
rs10491121 0.882 0.120 17 36102943 upstream gene variant G/A snv 0.32 5
rs4938723 0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 187
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 55
rs187115 0.695 0.320 11 35154612 intron variant T/C snv 0.37 22
rs3917356 0.882 0.160 2 112834786 intron variant C/T snv 0.39 4
rs6024836 0.851 0.160 20 56369012 downstream gene variant G/A snv 0.42 6
rs10877887 0.701 0.440 12 62603400 non coding transcript exon variant T/C snv 0.42 18
rs653765 0.763 0.240 15 58749813 upstream gene variant T/C;G snv 0.45 10
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs11077 0.732 0.320 6 43523209 3 prime UTR variant T/G snv 0.47 14
rs9679162 0.882 0.120 2 31024648 intron variant G/T snv 0.48 4
rs2071559
KDR
0.667 0.680 4 55126199 upstream gene variant A/G snv 0.53 26
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
rs1360485 0.742 0.320 13 30457747 3 prime UTR variant C/T snv 0.58 15
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 118
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
rs7628626 0.925 0.120 3 119525574 3 prime UTR variant A/C snv 0.82 2