CSNK2A1, casein kinase 2 alpha 1, 1457

N. diseases: 87; N. variants: 11
Disease: OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs869312846
rs869312846
Entrez Id: 1457
Gene Symbol: CSNK2A1
CSNK2A1
CUI: C4310739
Disease:
OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME 		G 0.700 CausalMutation CLINVAR