Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1554385305
rs1554385305
Entrez Id: 816
Gene Symbol: CAMK2B
CAMK2B
CUI: C4316870
Disease:
Abnormality of the eye
T 0.700 CausalMutation CLINVAR De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability. 29100089 2017