Source: CLINVAR

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 169522
Gene Symbol: KCNV2
KCNV2
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies 		0.100 CausalMutation CLINVAR Large deletions of the KCNV2 gene are common in patients with cone dystrophy with supernormal rod response. 21882291

2011
Entrez Id: 169522
Gene Symbol: KCNV2
KCNV2
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies 		0.100 GeneticVariation CLINVAR