RS767167623 HSD3B2
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What This Variant Does
"rs767167623, also known as c.867delG, represents a rare mutation in the HSD3B2 gene on chromosome 1."
Associated Conditions
3 beta-Hydroxysteroid dehydrogenase deficiency
3 beta-Hydroxysteroid dehydrogenase deficiency
Other Variants in HSD3B2