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rs80358220(A;C)

From SNPedia

Unaffected carrier of a 3HSDB2 deficiency mutation
Is agenotype
ofrs80358220
GeneHSD3B2
Chromosome1
Position119,422,165
mentionedby
Magnitude3
ReputeBad
Geno Mag Summary
(A;A) 7 3HSDB2 deficiency; congenital adrenal hyperplasia
(A;C) 3 Unaffected carrier of a 3HSDB2 deficiency mutation
(C;C) 0 common in clinvar

see discussion at HSD3B2