{{Rsnum
|rsid=62636519
|Chromosome=6
|Orientation=plus
|geno1=(-;-)
|geno2=(-;GTGCGGT)
|geno3=(GTGCGGT;GTGCGGT)
|Gene=PEX7
|position=136822683
|Gene_s=PEX7
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=AGTGCGGT
|CHROM=6
|CLNACC=RCV000008232.1; RCV000032115.1
|CLNALLE=1
|CLNDBN=Peroxisome biogenesis disorder 9B; Rhizomelic chondrodysplasia punctata type 1
|CLNDSDB=MedGen:OMIM:Orphanet; GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=CN159238:614879:773; NBK1270:C1859133:215100:177
|CLNHGVS=NC_000006.11:g.137143815_137143821dupGTGCGGT
|CLNORIGIN=0
|CLNSIG=5
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK1270; 601757.0010
|Disease=Peroxisome biogenesis disorder 9B; Rhizomelic chondrodysplasia punctata type 1
|FwdALT=GTGCGGT
|GENEINFO=PEX7:5191
|GENE_ID=5191
|GENE_NAME=PEX7
|REF=A
|RSPOS=137143807
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050168000000000002110200
|WGT=0
|dbSNPBuildID=129
|rsid=62636519
}}{{PMID Auto
|PMID=12522768
|Title=Identification of PEX7 as the second gene involved in Refsum disease.
|OA=1
}}