Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs25489 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78
rs754041352 1.000 0.080 19 43552051 missense variant G/A snv 1.2E-05 7.0E-06 1
rs774388757 1.000 0.080 19 43553421 missense variant C/T snv 2.0E-05 4.2E-05 1