{{Rsnum
|rsid=62641228
|Chromosome=22
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PEX26
|position=18079935
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PEX26
}}{{omim
|id=608666
|rsnum=62641228
|variant=0001
}}

{{ClinVar
|rsid=62641228
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=18562701
|CHROM=22
|dbSNPBuildID=129
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=PEX26:55670
|GENE_NAME=PEX26
|GENE_ID=55670
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000022.10:g.18562701C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=608666.0001
|CLNSIG=5
|CLNCUI=C0282525; C0282527
|CLNDBN=Peroxisome biogenesis disorder 7B
|Disease=Peroxisome biogenesis disorder 7B
|CLNACC=RCV000002234.1
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=CN159235:614873
}}

{{PMID|15858711|OA=1
}} Alternative splicing suggests extended function of PEX26 in peroxisome biogenesis.

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}