"NEI Ophthalmic Genomics Laboratory, National Institutes of Health"[su - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 46329	NM_032119.4(ADGRV1):c.4506C>T (p.Pro1502=)	ADGRV1	Single nucleotide variant (synonymous variant +1 more)	not provided +3 more	GBenign
Select item 46337	NM_032119.4(ADGRV1):c.5525-7C>T	ADGRV1	Single nucleotide variant (intron variant)	not provided +3 more	GBenign/Likely benign
Select item 46339	NM_032119.4(ADGRV1):c.5780C>T (p.Thr1927Met)	ADGRV1 (T1927M)	Single nucleotide variant (missense variant +1 more)	Usher syndrome type 2C +2 more	GBenign
Select item 46249	NM_032119.4(ADGRV1):c.10577T>C (p.Met3526Thr)	ADGRV1 (M3526T)	Single nucleotide variant (missense variant +1 more)	Usher syndrome type 2C +2 more	GBenign/Likely benign
Select item 46252	NM_032119.4(ADGRV1):c.10872A>G (p.Gln3624=)	ADGRV1	Single nucleotide variant (synonymous variant +1 more)	not provided +2 more	GBenign
Select item 100601	NM_032119.4(ADGRV1):c.16308C>A (p.Thr5436=)	ADGRV1	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign
Select item 100602	NM_032119.4(ADGRV1):c.18273A>G (p.Ala6091=)	ADGRV1	Single nucleotide variant (synonymous variant +1 more)	Febrile seizures, familial, 4 +3 more	GConflicting classifications of pathogenicity

ClinVar