{{Rsnum
|rsid=61753233
|Chromosome=6
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=PEX7
|position=136822705
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PEX7
}}{{omim
|id=601757
|rsnum=61753233
|variant=0011
}}{{ClinVar
|rsid=61753233
|Reversed=0
|FwdREF=A
|FwdALT=C
|REF=A
|ALT=C
|RSPOS=137143843
|CHROM=6
|dbSNPBuildID=129
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=PEX7:5191
|GENE_NAME=PEX7
|GENE_ID=5191
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000006.11:g.137143843A>C
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NBK1270; 601757.0011
|CLNSIG=5
|CLNCUI=C2749346
|CLNDBN=Peroxisome biogenesis disorder 9B; Rhizomelic chondrodysplasia punctata type 1
|Disease=Peroxisome biogenesis disorder 9B; Rhizomelic chondrodysplasia punctata type 1
|CLNACC=RCV000008233.1; RCV000032117.1
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet; GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=CN159238:614879:773; NBK1270:C1859133:215100:177
}}{{PMID Auto
|PMID=12522768
|Title=Identification of PEX7 as the second gene involved in Refsum disease.
|OA=1
}}