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rs121964897(C;C)

From SNPedia

common in clinvar
Is agenotype
ofrs121964897
GeneHSD3B2
Chromosome1
Position119,422,523
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 3 Unaffected carrier of a 3HSDB2 deficiency mutation
(T;T) 7 3HSDB2 deficiency; congenital adrenal hyperplasia