{{Rsnum
|rsid=199470486
|Chromosome=6
|Orientation=plus
|geno1=(-;-)
|geno2=(-;GGGACGCC)
|geno3=(GGGACGCC;GGGACGCC)
|Gene=PEX7
|position=136822717
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PEX7
}}{{ClinVar
|ALT=CGGGACGCC
|CHROM=6
|CLNACC=RCV000008226.1; RCV000032589.1
|CLNALLE=1
|CLNDBN=Rhizomelic chondrodysplasia punctata type 1; Peroxisome biogenesis disorder 9B
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1270:C1859133:215100:177; CN159238:614879:773
|CLNHGVS=NC_000006.11:g.137143848_137143855dupGGGACGCC
|CLNORIGIN=0
|CLNSIG=5
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK1270; 601757.0005
|Disease=Rhizomelic chondrodysplasia punctata type 1; Peroxisome biogenesis disorder 9B
|FwdALT=GGGACGCC
|REF=C
|RSPOS=137143847
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;S3D;SLO;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050360000000000002110200
|WGT=0
|dbSNPBuildID=136
|rsid=199470486
}}