RS770815049 HSD3B2

Health Risk Chr 1:119422056
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What This Variant Does
"rs770815049, also known as c.555_556insC and p.Thr187Hisfs, represents a rare mutation in the HSD3B2..."
Associated Conditions
3 beta-Hydroxysteroid dehydrogenase deficiency
3 beta-Hydroxysteroid dehydrogenase deficiency
Other Variants in HSD3B2
rs80358216 rs80358217 rs28934880 rs80358218 rs80358219 rs80358220 rs80358221 rs767167623 rs121964897 rs35887327
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