Variant: rs28940308 

    present in Gene: PEX26
    present in Chromosome: 22
    Position on Chromosome: 18079908
    Alleles of this Variant: G/A

rs28940308 in PEX26 gene and PEROXISOME BIOGENESIS DISORDER 7A (ZELLWEGER) PMID 12851857 2003 Mutations in novel peroxin gene PEX26 that cause peroxisome-biogenesis disorders of complementation group 8 provide a genotype-phenotype correlation.