{{Rsnum
|rsid=61753238
|Chromosome=6
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=PEX7
|position=136822785
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PEX7
}}{{omim
|id=601757
|rsnum=61753238
|variant=0009
}}

{{ClinVar
|rsid=61753238
|Reversed=0
|FwdREF=C
|FwdALT=G
|REF=C
|ALT=G
|RSPOS=137143923
|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.137143923C>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=601757.0009
|CLNSIG=5
|CLNCUI=C2749346; C1859133
|CLNDBN=Peroxisome biogenesis disorder 9B
|Disease=Peroxisome biogenesis disorder 9B
|CLNACC=RCV000008230.2
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=CN159238:614879:773
}}

{{PMID Auto
|PMID=12522768
|Title=Identification of PEX7 as the second gene involved in Refsum disease.
|OA=1
}}

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