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: rs1801262
rs1801262
4 0.882 0.120 2 181678728 missense variant T/C snv 0.70 0.68 0.080 0.750 8 1999 2013
dbSNP: rs8192556
rs8192556
2 0.925 0.120 2 181678271 missense variant G/T snv 1.9E-02 1.6E-02 0.010 1.000 1 2000 2000