CRYGC, crystallin gamma C, 1420

N. diseases: 60; N. variants: 13
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587778872
rs587778872
Entrez Id: 1420;100507443
Gene Symbol: CRYGC;LOC100507443
CRYGC;LOC100507443
CUI: C0026010
Disease:
Microphthalmos
A 0.700 CausalMutation CLINVAR