Variant: rs149806989 

    present in Gene: PEX1
    present in Chromosome: 7
    Position on Chromosome: 92517968
    Alleles of this Variant: G/A

rs149806989 in PEX1 gene and Infantile Refsum Disease (disorder) PMID 19105186 2009 Identification of novel mutations and sequence variation in the Zellweger syndrome spectrum of peroxisome biogenesis disorders.

rs149806989 in PEX1 gene and PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER) PMID 19105186 2009 Identification of novel mutations and sequence variation in the Zellweger syndrome spectrum of peroxisome biogenesis disorders.

rs149806989 in PEX1 gene and Peroxisome biogenesis disorders PMID 19105186 2009 Identification of novel mutations and sequence variation in the Zellweger syndrome spectrum of peroxisome biogenesis disorders.

PMID 19877282 2010 Spectrum of PEX6 mutations in Zellweger syndrome spectrum patients.