"Clinical Genetics, Academic Medical Center"[submitter] AND "CRX"[gene - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 7418	NM_000554.6(CRX):c.121C>T (p.Arg41Trp)	CRX (R41W)	Single nucleotide variant (missense variant)	Retinal dystrophy +4 more	GPathogenic
Select item 99597	NM_000554.6(CRX):c.196G>A (p.Val66Ile)	CRX (V66I)	Single nucleotide variant (missense variant)	Retinal dystrophy +6 more	GBenign/Likely benign
Select item 99600	NM_000554.6(CRX):c.253-15G>A	CRX	Single nucleotide variant (intron variant)	Cone-rod dystrophy 2 +3 more	GConflicting classifications of pathogenicity

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