"Genetic Services Laboratory, University of Chicago"[submitter] AND "N - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 436028	NM_000475.5(NR0B1):c.1365A>G (p.Thr455=)	NR0B1	Single nucleotide variant (synonymous variant)	not specified +3 more	GBenign/Likely benign
Select item 703336	NM_000475.5(NR0B1):c.1029G>A (p.Leu343=)	NR0B1	Single nucleotide variant (synonymous variant)	not specified +3 more	GBenign/Likely benign
Select item 1336216	NM_000475.5(NR0B1):c.344T>C (p.Val115Ala)	NR0B1 (V115A)	Single nucleotide variant (missense variant)	Congenital adrenal hypoplasia, X-linked +2 more	GBenign

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ClinVar