CRYAA, crystallin alpha A, 1409

N. diseases: 40; N. variants: 18
Disease: Myopia ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs397515624
rs397515624
Entrez Id: 1409;107987300
Gene Symbol: CRYAA;LOC107987300
CRYAA;LOC107987300
CUI: C0027092
Disease:
Myopia 		0.010 GeneticVariation BEFREE Elongation of axial length accompanied with myopia was a novel phenotype in the family with the c.34C>T mutation in CRYAA. 21686328 2011