ClinVar for OMIM (Select 190900) - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1411010	NM_001385125.1(OPN1SW):c.173G>A (p.Arg58His)	OPN1SW (R58H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1169097	NM_001385125.1(OPN1SW):c.357A>C (p.Gly119=)	OPN1SW	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 64	NM_001708.2(OPN1SW):c.790C>T (p.Pro264Ser)	OPN1SW	Single nucleotide variant	not provided	GUncertain significance
Select item 63	NM_001708.2(OPN1SW):c.640T>C (p.Ser214Pro)	OPN1SW	Single nucleotide variant	not provided	GUncertain significance
Select item 62	NM_001708.2(OPN1SW):c.235G>A (p.Gly79Arg)	OPN1SW	Single nucleotide variant	not provided	GLikely benign

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