Variant: rs431905504 

    present in Gene: SLC6A3
    present in Chromosome: 5
    Position on Chromosome: 1411242
    Alleles of this Variant: C/T

rs431905504 in SLC6A3 gene and Extrapyramidal sign PMID 22279524 2012 Genetic mapping and exome sequencing identify variants associated with five novel diseases.

rs431905504 in SLC6A3 gene and Febrile Convulsions PMID 22279524 2012 Genetic mapping and exome sequencing identify variants associated with five novel diseases.

rs431905504 in SLC6A3 gene and Global developmental delay PMID 22279524 2012 Genetic mapping and exome sequencing identify variants associated with five novel diseases.

rs431905504 in SLC6A3 gene and Hip Dysplasia PMID 22279524 2012 Genetic mapping and exome sequencing identify variants associated with five novel diseases.

rs431905504 in SLC6A3 gene and PARKINSONISM-DYSTONIA, INFANTILE, 1 PMID 22279524 2012 Genetic mapping and exome sequencing identify variants associated with five novel diseases.

rs431905504 in SLC6A3 gene and Pediatric failure to thrive PMID 22279524 2012 Genetic mapping and exome sequencing identify variants associated with five novel diseases.

rs431905504 in SLC6A3 gene and Quadriplegia PMID 22279524 2012 Genetic mapping and exome sequencing identify variants associated with five novel diseases.

rs431905504 in SLC6A3 gene and Scoliosis, unspecified PMID 22279524 2012 Genetic mapping and exome sequencing identify variants associated with five novel diseases.

rs431905504 in SLC6A3 gene and Spina Bifida Occulta PMID 22279524 2012 Genetic mapping and exome sequencing identify variants associated with five novel diseases.