"Clinical Genetics, Academic Medical Center"[submitter] AND "KCNV2"[ge - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 914190	NM_133497.4(KCNV2):c.258C>G (p.Pro86=)	KCNV2	Single nucleotide variant (synonymous variant)	Cone dystrophy with supernormal rod response +2 more	GConflicting classifications of pathogenicity
Select item 96359	NM_133497.4(KCNV2):c.312T>C (p.Gly104=)	KCNV2	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign
Select item 498304	NM_133497.4(KCNV2):c.645G>C (p.Lys215Asn)	KCNV2 (K215N)	Single nucleotide variant (missense variant)	not specified +3 more	GBenign/Likely benign
Select item 96360	NM_133497.4(KCNV2):c.676G>A (p.Val226Ile)	KCNV2 (V226I)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign
Select item 718563	NM_133497.4(KCNV2):c.828G>A (p.Ala276=)	KCNV2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1284705	NM_133497.4(KCNV2):c.1162C>G (p.Leu388Val)	KCNV2 (L388V)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance

ClinVar