Variant: rs724160002 

    present in Gene: PLCH2;PEX10
    present in Chromosome: 1
    Position on Chromosome: 2412501
    Alleles of this Variant: A/G

rs724160002 in PLCH2;PEX10 gene and PEROXISOME BIOGENESIS DISORDER 6A (ZELLWEGER) PMID 21031596 2011 Genetic classification and mutational spectrum of more than 600 patients with a Zellweger syndrome spectrum disorder.

PMID 20695019 2010 Mutations in PEX10 are a cause of autosomal recessive ataxia.

rs724160002 in PLCH2;PEX10 gene and PEROXISOME BIOGENESIS DISORDER 6B PMID 20695019 2010 Mutations in PEX10 are a cause of autosomal recessive ataxia.

PMID 21031596 2011 Genetic classification and mutational spectrum of more than 600 patients with a Zellweger syndrome spectrum disorder.