"Clinical Genetics, Academic Medical Center"[submitter] AND "VCAN-AS1" - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 167822	NM_004385.5(VCAN):c.5187G>A (p.Glu1729=)	VCAN, VCAN-AS1	Single nucleotide variant (synonymous variant +1 more)	not specified +3 more	GBenign/Likely benign
Select item 198801	NM_004385.5(VCAN):c.6902T>G (p.Phe2301Cys)	VCAN, VCAN-AS1 (F2301C +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +2 more	GConflicting classifications of pathogenicity
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 354444	NM_004385.5(VCAN):c.7551C>T (p.Asp2517=)	VCAN, VCAN-AS1	Single nucleotide variant (synonymous variant +1 more)	Vitreoretinopathy +2 more	GBenign/Likely benign
Select item 354445	NM_004385.5(VCAN):c.7581C>T (p.Phe2527=)	VCAN, VCAN-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided +2 more	GBenign/Likely benign
Select item 198806	NM_004385.5(VCAN):c.8621C>T (p.Ala2874Val)	VCAN, VCAN-AS1 (A2874V +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GConflicting classifications of pathogenicity
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

ClinVar