Gene: CLCN4 ×
Source: INFERRED ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587777161
rs587777161
CLCN4
C 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
dbSNP: rs879255580
rs879255580
CLCN4
G 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
dbSNP: rs879255581
rs879255581
CLCN4
C 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
dbSNP: rs879255582
rs879255582
CLCN4
T 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
dbSNP: rs879255583
rs879255583
CLCN4
T 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
dbSNP: rs879255584
rs879255584
CLCN4
T 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
dbSNP: rs879255585
rs879255585
CLCN4
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
dbSNP: rs879255586
rs879255586
CLCN4
CA 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
dbSNP: rs879255590
rs879255590
CLCN4
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