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rs770815049(-;C)

From SNPedia

Unaffected carrier of a 3HSDB2 deficiency mutation
Is agenotype
ofrs770815049
GeneHSD3B2
Chromosome1
Position119,422,056
mentionedby
Magnitude3
ReputeBad
Geno Mag Summary
(-;-) 0 common/normal
(-;C) 3 Unaffected carrier of a 3HSDB2 deficiency mutation
(C;C) 7 3HSDB2 deficiency; congenital adrenal hyperplasia

see discussion at HSD3B2