Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs200805087
rs200805087
Entrez Id: 54714
Gene Symbol: CNGB3
CNGB3
CUI: C1849792
Disease:
Achromatopsia 3
A 0.700 CausalMutation CLINVAR