{{Rsnum
|rsid=121909154
|Chromosome=6
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=PEX7
|position=136845620
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PEX7
}}{{omim
|id=601757
|rsnum=121909154
|variant=0007
}}{{ClinVar
|rsid=121909154
|Reversed=0
|FwdREF=T
|FwdALT=G
|REF=T
|ALT=G
|RSPOS=137166758
|CHROM=6
|dbSNPBuildID=133
|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.137166758T>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=601757.0007
|CLNSIG=5
|CLNCUI=C2749346
|CLNDBN=Peroxisome biogenesis disorder 9B
|Disease=Peroxisome biogenesis disorder 9B
|CLNACC=RCV000008228.1
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=CN159238:614879:773
}}{{PMID Auto
|PMID=12325024
|Title=Mutation analysis of PEX7 in 60 probands with rhizomelic chondrodysplasia punctata and functional correlations of genotype with phenotype.
}}