Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4149056 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 45
rs4148323 0.701 0.440 2 233760498 missense variant G/A snv 2.2E-02 9.2E-03 22
rs1042640 1.000 0.080 2 233772898 3 prime UTR variant G/A;C;T snv 3
rs10929303 1.000 0.080 2 233772770 3 prime UTR variant T/C snv 0.74 3