{{Rsnum
|rsid=61752123
|Chromosome=8
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PEX2
|position=76983824
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PEX2
}}{{omim
|id=170993
|rsnum=61752123
|variant=0001
}}{{ClinVar
|rsid=61752123
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=77896060
|CHROM=8
|dbSNPBuildID=129
|SSR=0
|SAO=1
|VP=0x050168000000040002110100
|GENEINFO=PEX2:5828
|GENE_NAME=PEX2
|GENE_ID=5828
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000008.10:g.77896060G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=170993.0001
|CLNSIG=5
|CLNCUI=CN069920
|CLNDBN=Peroxisome biogenesis disorder 5A; Peroxisome biogenesis disorder 5B
|Disease=Peroxisome biogenesis disorder 5A; Peroxisome biogenesis disorder 5B
|CLNACC=RCV000014703.18; RCV000032924.18
|Tags=RV;PM;PMC;SLO;VLD;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet; MedGen:OMIM
|CLNDSDBID=CN159230:614866:912; CN159231:614867
}}{{PMID Auto
|PMID=9585609
|Title=Temperature-sensitive phenotypes of peroxisome-assembly processes represent the milder forms of human peroxisome-biogenesis disorders.
|OA=1
}}