Disease: Retinal Cone Dystrophy 3B ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894113
rs104894113
Entrez Id: 169522
Gene Symbol: KCNV2
KCNV2
CUI: C1835897
Disease:
Retinal Cone Dystrophy 3B 		T 0.700 CausalMutation CLINVAR