CRYGC, crystallin gamma C, 1420

N. diseases: 60; N. variants: 13
Disease: Crystalline cataract ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1040762144
rs1040762144
Entrez Id: 1420;100507443
Gene Symbol: CRYGC;LOC100507443
CRYGC;LOC100507443
CUI: C1392110
Disease:
Crystalline cataract 		0.010 GeneticVariation BEFREE The heterozygous 109C→A CRYGD missense mutation is associated with a distinct crystalline cataract in two US Caucasian pedigrees. 22219628 2011