{{Rsnum
|rsid=121909152
|Chromosome=6
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=PEX7
|position=136869905
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PEX7
}}{{omim
|id=601757
|rsnum=121909152
|variant=0003
}}{{ClinVar
|rsid=121909152
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=137191043
|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.137191043G>A
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NBK1270; 601757.0003
|CLNSIG=5
|CLNCUI=C1859133
|CLNDBN=Rhizomelic chondrodysplasia punctata type 1
|Disease=Rhizomelic chondrodysplasia punctata type 1
|CLNACC=RCV000008224.1
|Tags=PM;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1270:C1859133:215100:177
}}