"Clinical Genetics, Academic Medical Center"[submitter] AND "OPN1LW"[g - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 10504	NM_020061.6(OPN1LW):c.538= (p.Ala180=)	OPN1LW	Single nucleotide variant (no sequence alteration)	RED CONE POLYMORPHISM +2 more	GBenign/Likely benign
Select item 1284461	NM_020061.6(OPN1LW):c.957C>T (p.Pro319=)	OPN1LW	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign