SLC9A6, solute carrier family 9 member A6, 10479

N. diseases: 210; N. variants: 15
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1556617455
rs1556617455
Entrez Id: 10479
Gene Symbol: SLC9A6
SLC9A6
CUI: C2678194
Disease:
Mental Retardation, X-Linked, Syndromic, Christianson Type
A 0.700 GeneticVariation CLINVAR SLC9A6 mutations cause X-linked mental retardation, microcephaly, epilepsy, and ataxia, a phenotype mimicking Angelman syndrome. 18342287 2008
dbSNP: rs1057519394
rs1057519394
Entrez Id: 10479
Gene Symbol: SLC9A6
SLC9A6
CUI: C2678194
Disease:
Mental Retardation, X-Linked, Syndromic, Christianson Type
G 0.700 CausalMutation CLINVAR
dbSNP: rs1057519394
rs1057519394
Entrez Id: 10479
Gene Symbol: SLC9A6
SLC9A6
CUI: C1843367
Disease:
Poor school performance
G 0.700 CausalMutation CLINVAR
dbSNP: rs1064793575
rs1064793575
Entrez Id: 10479
Gene Symbol: SLC9A6
SLC9A6
CUI: C0036439
Disease:
Scoliosis, unspecified
C 0.700 GeneticVariation CLINVAR
dbSNP: rs1064793575
rs1064793575
Entrez Id: 10479
Gene Symbol: SLC9A6
SLC9A6
CUI: C0557874
Disease:
Global developmental delay
C 0.700 GeneticVariation CLINVAR
dbSNP: rs1064793575
rs1064793575
Entrez Id: 10479
Gene Symbol: SLC9A6
SLC9A6
CUI: C3806482
Disease:
Recurrent respiratory infections
C 0.700 GeneticVariation CLINVAR
dbSNP: rs1064793575
rs1064793575
Entrez Id: 10479
Gene Symbol: SLC9A6
SLC9A6
CUI: C0037317
Disease:
Sleep disturbances
C 0.700 GeneticVariation CLINVAR
dbSNP: rs1064793575
rs1064793575
Entrez Id: 10479
Gene Symbol: SLC9A6
SLC9A6
CUI: C0036572
Disease:
Seizures
C 0.700 GeneticVariation CLINVAR
dbSNP: rs1064793575
rs1064793575
Entrez Id: 10479
Gene Symbol: SLC9A6
SLC9A6
CUI: C4023342
Disease:
Gastrostomy tube feeding in infancy
C 0.700 GeneticVariation CLINVAR
dbSNP: rs122461162
rs122461162
Entrez Id: 10479
Gene Symbol: SLC9A6
SLC9A6
CUI: C2678194
Disease:
Mental Retardation, X-Linked, Syndromic, Christianson Type
T 0.700 CausalMutation CLINVAR
dbSNP: rs1569525357
rs1569525357
Entrez Id: 10479
Gene Symbol: SLC9A6
SLC9A6
CUI: C2678194
Disease:
Mental Retardation, X-Linked, Syndromic, Christianson Type
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1569525894
rs1569525894
Entrez Id: 10479
Gene Symbol: SLC9A6
SLC9A6
CUI: C4021798
Disease:
Impaired use of nonverbal behaviors
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1569525894
rs1569525894
Entrez Id: 10479
Gene Symbol: SLC9A6
SLC9A6
CUI: C0423224
Disease:
Sunken eyes
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1569525894
rs1569525894
Entrez Id: 10479
Gene Symbol: SLC9A6
SLC9A6
CUI: C1850049
Disease:
Clinodactyly of the 5th finger
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1569525894
rs1569525894
Entrez Id: 10479
Gene Symbol: SLC9A6
SLC9A6
CUI: C1858120
Disease:
Generalized hypotonia
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1569525894
rs1569525894
Entrez Id: 10479
Gene Symbol: SLC9A6
SLC9A6
CUI: C2315100
Disease:
Pediatric failure to thrive
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1569525894
rs1569525894
Entrez Id: 10479
Gene Symbol: SLC9A6
SLC9A6
CUI: C0431352
Disease:
Secondary microcephaly
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1569525894
rs1569525894
Entrez Id: 10479
Gene Symbol: SLC9A6
SLC9A6
CUI: C0004352
Disease:
Autistic Disorder
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1569525894
rs1569525894
Entrez Id: 10479
Gene Symbol: SLC9A6
SLC9A6
CUI: C4024946
Disease:
Focal white matter lesions
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1569525894
rs1569525894
Entrez Id: 10479
Gene Symbol: SLC9A6
SLC9A6
CUI: C0557874
Disease:
Global developmental delay
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1569525894
rs1569525894
Entrez Id: 10479
Gene Symbol: SLC9A6
SLC9A6
CUI: C0349588
Disease:
Short stature
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1569525894
rs1569525894
Entrez Id: 10479
Gene Symbol: SLC9A6
SLC9A6
CUI: C0016842
Disease:
Congenital pectus excavatum
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1569525894
rs1569525894
Entrez Id: 10479
Gene Symbol: SLC9A6
SLC9A6
CUI: C0008489
Disease:
Chorea
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1569525894
rs1569525894
Entrez Id: 10479
Gene Symbol: SLC9A6
SLC9A6
CUI: C0036572
Disease:
Seizures
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1569525894
rs1569525894
Entrez Id: 10479
Gene Symbol: SLC9A6
SLC9A6
CUI: C0014877
Disease:
Esotropia
A 0.700 GeneticVariation CLINVAR