C3887938[trait identifier] AND "OMIM"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 10510	NM_000513.2(OPN1MW):c.-112A>C	OPN1MW	Single nucleotide variant	Deuteranomaly	GPathogenic
Select item 10512	NM_000513.2(OPN1MW):c.282C>A (p.Asn94Lys)	OPN1MW (N94K)	Single nucleotide variant (missense variant)	Deuteranomaly	GPathogenic
Select item 10509	NM_000513.2(OPN1MW):c.989G>A (p.Arg330Gln)	OPN1MW (R330Q)	Single nucleotide variant (missense variant)	Deuteranomaly	GPathogenic

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