rs1569525894, SLC9A6

N. diseases: 14
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Impaired use of nonverbal behaviors
CUI: C4021798
Disease: Impaired use of nonverbal behaviors
0.700 GeneticVariation CLINVAR
Sunken eyes
CUI: C0423224
Disease: Sunken eyes
0.700 GeneticVariation CLINVAR
Clinodactyly of the 5th finger
CUI: C1850049
Disease: Clinodactyly of the 5th finger
0.700 GeneticVariation CLINVAR
Generalized hypotonia
CUI: C1858120
Disease: Generalized hypotonia
0.700 GeneticVariation CLINVAR
Pediatric failure to thrive
CUI: C2315100
Disease: Pediatric failure to thrive
0.700 GeneticVariation CLINVAR
Secondary microcephaly
CUI: C0431352
Disease: Secondary microcephaly
0.700 GeneticVariation CLINVAR
Autistic Disorder
CUI: C0004352
Disease: Autistic Disorder
0.700 GeneticVariation CLINVAR
Focal white matter lesions
CUI: C4024946
Disease: Focal white matter lesions
0.700 GeneticVariation CLINVAR
Global developmental delay
CUI: C0557874
Disease: Global developmental delay
0.700 GeneticVariation CLINVAR
Short stature
CUI: C0349588
Disease: Short stature
0.700 GeneticVariation CLINVAR
Congenital pectus excavatum
CUI: C0016842
Disease: Congenital pectus excavatum
0.700 GeneticVariation CLINVAR
Chorea
CUI: C0008489
Disease: Chorea
0.700 GeneticVariation CLINVAR
Seizures
CUI: C0036572
Disease: Seizures
0.700 GeneticVariation CLINVAR
Esotropia
CUI: C0014877
Disease: Esotropia
0.700 GeneticVariation CLINVAR