Disease: Achromatopsia ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs201794629
rs201794629
Entrez Id: 54714
Gene Symbol: CNGB3
CNGB3
CUI: C0152200
Disease:
Achromatopsia 		G 0.700 CausalMutation CLINVAR