Gene: CYP21A2 ×
Source: CLINVAR ×
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: rs117905900
rs117905900
CFB ; CYP21A2
1 0.925 0.120 6 31948042 missense variant C/G;T snv 1.1E-02 0.800 1.000 0 2009 2010
dbSNP: rs121909748
rs121909748
CFB ; CYP21A2
1 0.925 0.120 6 31948443 missense variant A/G snv 0.800 1.000 0 2007 2010