Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs752298579 0.701 0.480 22 20061538 missense variant G/A snv 1.4E-04 7.0E-06 48
rs61755320 0.716 0.520 16 89546737 missense variant C/T snv 2.9E-03 3.5E-03 41
rs1043679457 0.752 0.400 5 60927745 intron variant C/A;G;T snv 33
rs1217391623 0.882 0.160 16 89556976 frameshift variant G/- del 7.0E-06 11
rs768823392 0.827 0.120 16 89546657 coding sequence variant GGCGGGAGA/- delins 2.6E-04 4.2E-04 10
rs1561904557 0.851 0.160 5 150056050 missense variant GGAT/TGCC mnv 9