"PreventionGenetics, part of Exact Sciences"[submitter] AND "OPN1SW"[g - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1167587	NM_001385125.1(OPN1SW):c.1014G>T (p.Ser338=)	CALU, OPN1SW	Single nucleotide variant (synonymous variant +2 more)	OPN1SW-related disorder +1 more	GBenign/Likely benign
Select item 1170089	NM_001385125.1(OPN1SW):c.895A>G (p.Ile299Val)	OPN1SW (I299V)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 1081214	NM_001385125.1(OPN1SW):c.678+5del	OPN1SW	Deletion (intron variant)	OPN1SW-related disorder +1 more	GLikely benign
Select item 1097460	NM_001385125.1(OPN1SW):c.561C>T (p.Thr187=)	OPN1SW	Single nucleotide variant (synonymous variant)	OPN1SW-related disorder +1 more	GLikely benign
Select item 1169097	NM_001385125.1(OPN1SW):c.357A>C (p.Gly119=)	OPN1SW	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign
Select item 1085426	NM_001385125.1(OPN1SW):c.51G>A (p.Pro17=)	OPN1SW	Single nucleotide variant (synonymous variant)	OPN1SW-related disorder +1 more	GLikely benign
Select item 1166132	NM_001385125.1(OPN1SW):c.6G>A (p.Ser2=)	OPN1SW	Single nucleotide variant (synonymous variant)	OPN1SW-related disorder +1 more	GBenign/Likely benign

ClinVar