{{Rsnum
|rsid=62636524
|Chromosome=1
|Orientation=minus
|geno1=(-;-)
|geno2=(-;G)
|geno3=(G;G)
|Gene=PEX10
|position=2412499
|Gene_s=PEX10
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=62636524
|Reversed=1
|FwdREF=G
|FwdALT=
|REF=GC
|ALT=G
|RSPOS=2343937
|CHROM=1
|dbSNPBuildID=129
|SSR=0
|SAO=1
|VP=0x050168001201000002100200
|GENEINFO=PEX10:5192
|GENE_NAME=PEX10
|GENE_ID=5192
|WGT=1
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000001.10:g.2343938delC
|CLNORIGIN=0
|CLNSIG=1
|Tags=RV;PM;PMC;SLO;NSF;REF;OTHERKG;LSD
|FwdALT=
|RS=62636524
|FwdALT=
}}{{PMID|15542397}} The PEX Gene Screen: molecular diagnosis of peroxisome biogenesis disorders in the Zellweger syndrome spectrum.