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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NR0B1
(W236*)
Single nucleotide variant
(nonsense)
Congenital adrenal hypoplasia, X-linked
+2 more
GPathogenic
NR0B1
(Y91*)
Single nucleotide variant
(nonsense)
not provided
GPathogenic