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rs80358219(A;G)

From SNPedia

Unaffected carrier of a 3HSDB2 deficiency mutation
Is agenotype
ofrs80358219
GeneHSD3B2
Chromosome1
Position119,421,925
mentionedby
Magnitude3
ReputeBad
Geno Mag Summary
(A;A) 7 3HSDB2 deficiency; congenital adrenal hyperplasia
(G;G) 0 common in clinvar

see discussion at HSD3B2