RS767167623 HSD3B2

Health Risk Chr 1:119422368
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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
rs80358216 rs770815049 rs80358217 rs28934880 rs80358218 rs80358219 rs80358220 rs80358221 rs121964897 rs35887327
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