CRYGD, crystallin gamma D, 1421

N. diseases: 168; N. variants: 18
Disease: Cataract ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs150857132
rs150857132
Entrez Id: 1421;100507443
Gene Symbol: CRYGD;LOC100507443
CRYGD;LOC100507443
CUI: C0086543
Disease:
Cataract 		0.010 GeneticVariation BEFREE Mutation G61C in the CRYGD gene causing autosomal dominant congenital coralliform cataracts. 18334953 2008