Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs879255590
rs879255590
Entrez Id: 1183
Gene Symbol: CLCN4
CLCN4
CUI: C1843367
Disease:
Poor school performance
A 0.700 CausalMutation CLINVAR De novo and inherited mutations in the X-linked gene CLCN4 are associated with syndromic intellectual disability and behavior and seizure disorders in males and females. 27550844 2018