Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1799853
rs1799853
11 0.763 0.320 10 94942290 missense variant C/T snv 9.2E-02 8.9E-02 0.020 1.000 2 2006 2014
dbSNP: rs1057910
rs1057910
12 0.776 0.280 10 94981296 missense variant A/C;G snv 6.3E-02; 4.0E-06 0.010 1.000 1 2006 2006
dbSNP: rs150435881
rs150435881
1 1.000 0.080 10 94947853 missense variant C/A;T snv 4.0E-06; 5.6E-05 0.010 1.000 1 2006 2006