"Genome Diagnostics Laboratory, Amsterdam University Medical Center"[s - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 259361	NM_004385.5(VCAN):c.1283G>A (p.Gly428Asp)	VCAN (G428D)	Single nucleotide variant (missense variant +1 more)	Vitreoretinopathy +3 more	GBenign
Select item 354398	NM_004385.5(VCAN):c.1523T>A (p.Ile508Asn)	VCAN (I508N)	Single nucleotide variant (missense variant +1 more)	Vitreoretinopathy +2 more	GBenign/Likely benign
Select item 728947	NM_004385.5(VCAN):c.2887C>T (p.Pro963Ser)	VCAN (P963S)	Single nucleotide variant (missense variant +1 more)	Vitreoretinopathy +2 more	GBenign
Select item 167821	NM_004385.5(VCAN):c.4604A>G (p.Glu1535Gly)	VCAN, VCAN-AS1 (E1535G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified +3 more	GBenign/Likely benign
Select item 354440	NM_004385.5(VCAN):c.7419C>T (p.Ser2473=)	VCAN, VCAN-AS1	Single nucleotide variant (synonymous variant +1 more)	Vitreoretinopathy +2 more	GBenign/Likely benign
Select item 259376	NM_004385.5(VCAN):c.9234G>A (p.Glu3078=)	VCAN, VCAN-AS1	Single nucleotide variant (synonymous variant +1 more)	not specified +3 more	GBenign/Likely benign
Select item 259379	NM_004385.5(VCAN):c.9882C>T (p.Val3294=)	VCAN	Single nucleotide variant (synonymous variant)	Vitreoretinopathy +3 more	GBenign

ClinVar