Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs770374710 0.611 0.560 15 23645747 frameshift variant G/-;GG delins 87
rs1085307993 0.716 0.440 5 161331056 missense variant C/T snv 53
rs752746786 0.742 0.560 1 1806503 missense variant A/C;G;T snv 4.0E-06 30
rs869312824 0.827 0.200 1 1804565 missense variant A/G snv 14
rs869025195 0.790 0.280 1 155904493 missense variant T/G snv 11
rs869312823 0.882 0.080 1 1806509 missense variant T/C snv 9
rs1057518681 0.827 0.200 8 143816821 splice acceptor variant T/C snv 7