Variant: rs1357615935 

    present in Gene: SLC20A2
    present in Chromosome: 8
    Position on Chromosome: 42437211
    Alleles of this Variant: G/C

rs1357615935 in SLC20A2 gene and Idiopathic basal ganglia calcification 1 PMID 23334463 2013 Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification.

PMID 25284758 2014 Primary familial brain calcification: Genetic analysis and clinical spectrum.

PMID 23406454 2013 Reporting a new mutation at the SLC20A2 gene in familial idiopathic basal ganglia calcification.

PMID 23939468 2013 Novel SLC20A2 mutations identified in southern Chinese patients with idiopathic basal ganglia calcification.

PMID 15955065 2005 Evolutionary and experimental analyses of inorganic phosphate transporter PiT family reveals two related signature sequences harboring highly conserved aspartic acids critical for sodium-dependent phosphate transport function of human PiT2.

PMID 24463626 2014 Evaluation of SLC20A2 mutations that cause idiopathic basal ganglia calcification in Japan.

PMID 22327515 2012 Mutations in SLC20A2 link familial idiopathic basal ganglia calcification with phosphate homeostasis.

PMID 24065723 2013 Phenotypic spectrum of probable and genetically-confirmed idiopathic basal ganglia calcification.