{{Rsnum
|rsid = 28939678
|Gene = PEX1
|Orientation=minus
|ReferenceAllele=T
|MissenseAllele=C
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Chromosome=7
|position=92504812
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Status=Merged
|Merged=121434455
|Gene_s=PEX1
}}{{omim
| id = 602136
| variant = 0002
| desc    = ZELLWEGER SYNDROME
| rsnum   = 28939678
}}{{PMID|11439091|OA=1
}} Phenotype-genotype relationships in peroxisome biogenesis disorders of PEX1-defective complementation group 1 are defined by Pex1p-Pex6p interaction.