"3billion"[submitter] AND "KCNV2"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1333382	NM_133497.4(KCNV2):c.617G>C (p.Arg206Pro)	KCNV2 (R206P)	Single nucleotide variant (missense variant)	Cone dystrophy with supernormal rod response	GUncertain significance
Select item 1333521	NM_133497.4(KCNV2):c.719G>A (p.Gly240Asp)	KCNV2 (G240D)	Single nucleotide variant (missense variant)	Cone dystrophy with supernormal rod response +1 more	GUncertain significance