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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NR0B1
(C200W)
Single nucleotide variant
(missense variant)
Congenital adrenal hypoplasia, X-linked
+1 more
GBenign/Likely benign
NR0B1
(V126M)
Single nucleotide variant
(missense variant)
not specified
+4 more
GConflicting classifications of pathogenicity