{{Rsnum
|rsid=61752092
|Chromosome=1
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PEX10
|position=2406766
|Gene_s=PEX10
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=61752092
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=2338205
|CHROM=1
|dbSNPBuildID=129
|SSR=0
|SAO=1
|VP=0x050168000601000002100100
|GENEINFO=PEX10:5192
|GENE_NAME=PEX10
|GENE_ID=5192
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.10:g.2338205G>A
|CLNORIGIN=0
|CLNSIG=1
|Tags=RV;PM;PMC;SLO;NSN;REF;OTHERKG;LSD
|RS=61752092
}}

{{PMID Auto
|PMID=15542397
|Title=The PEX Gene Screen: molecular diagnosis of peroxisome biogenesis disorders in the Zellweger syndrome spectrum.
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}