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: rs1801278
rs1801278
38 0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 0.100 0.833 18 2001 2017
dbSNP: rs1801276
rs1801276
3 0.882 0.160 2 226797205 missense variant C/G snv 1.4E-02 1.3E-02 0.010 < 0.001 1 2006 2006
dbSNP: rs764352157
rs764352157
2 0.925 0.160 2 226797914 synonymous variant G/A snv 4.0E-06 1.4E-05 0.010 1.000 1 2010 2010