CRYGD, crystallin gamma D, 1421

N. diseases: 168; N. variants: 18
Disease: Congenital cataract ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs770593386
rs770593386
Entrez Id: 1421;100507443
Gene Symbol: CRYGD;LOC100507443
CRYGD;LOC100507443
CUI: C0009691
Disease:
Congenital cataract 		0.010 GeneticVariation BEFREE A novel rare variant in CRYGD (Y134C) was detected in a Brazilian family with congenital cataract. 21866214 2011