{{Rsnum
|rsid=121909151
|Chromosome=6
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PEX7
|position=136869909
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PEX7
}}{{omim
|id=601757
|rsnum=121909151
|variant=0002
}}{{ClinVar
|rsid=121909151
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=137191047
|CHROM=6
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050360000000000002110100
|GENEINFO=PEX7:5191
|GENE_NAME=PEX7
|GENE_ID=5191
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000006.11:g.137191047C>T
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1270; 601757.0002
|CLNSIG=5
|CLNCUI=C1859133
|CLNDBN=Rhizomelic chondrodysplasia punctata type 1; Peroxisome biogenesis disorder 9B
|Disease=Rhizomelic chondrodysplasia punctata type 1; Peroxisome biogenesis disorder 9B
|CLNACC=RCV000008223.2; RCV000032925.1
|Tags=PM;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1270:C1859133:215100:177; CN159238:614879:773
}}