Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs397515626
rs397515626
Entrez Id: 1409;107987300
Gene Symbol: CRYAA;LOC107987300
CRYAA;LOC107987300
CUI: C1858679
Disease:
CATARACT, AUTOSOMAL DOMINANT
A 0.700 CausalMutation CLINVAR