CRYGC, crystallin gamma C, 1420

N. diseases: 60; N. variants: 13
Disease: CATARACT 2, MULTIPLE TYPES ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs398122944
rs398122944
Entrez Id: 1420;100507443
Gene Symbol: CRYGC;LOC100507443
CRYGC;LOC100507443
CUI: C4721890
Disease:
CATARACT 2, MULTIPLE TYPES 		T 0.700 CausalMutation CLINVAR