Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs2071559
KDR
0.667 0.680 4 55126199 upstream gene variant A/G snv 0.53 26
rs7813 0.689 0.360 17 744946 missense variant G/A;C snv 0.63 22
rs4402960 0.724 0.400 3 185793899 intron variant G/T snv 0.38 21
rs3809865 0.790 0.240 17 47311220 3 prime UTR variant T/A;G snv 11
rs636832 0.790 0.400 1 35897874 intron variant G/A snv 0.23 8
rs17664 0.882 0.120 2 172504503 3 prime UTR variant A/G;T snv 4
rs2675 0.882 0.120 3 124763266 3 prime UTR variant T/G snv 0.17 4