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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HSD3B2
(P222T)
Single nucleotide variant
(missense variant)
Congenital adrenal hyperplasia
+1 more
GPathogenic
HSD3B2
(W292*)
Single nucleotide variant
(nonsense)
3 beta-Hydroxysteroid dehydrogenase deficiency
GLikely pathogenic
HSD3B2
(Q334*)
Single nucleotide variant
(nonsense)
not provided
+1 more
GPathogenic/Likely pathogenic
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