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: rs869312845
rs869312845
Entrez Id: 1457
Gene Symbol: CSNK2A1
CSNK2A1
CUI: C4310739
Disease:
OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME 		0.800 GeneticVariation UNIPROT De novo mutations in CSNK2A1 are associated with neurodevelopmental abnormalities and dysmorphic features. 27048600 2016
dbSNP: rs869312845
rs869312845
Entrez Id: 1457
Gene Symbol: CSNK2A1
CSNK2A1
CUI: C4310739
Disease:
OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME 		T 0.800 CausalMutation CLINVAR