{{Rsnum
|rsid=61750434
|Chromosome=1
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PEX10
|position=2408679
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PEX10
}}{{omim
|id=602859
|rsnum=61750434
|variant=0003
}}

{{ClinVar
|rsid=61750434
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=2408679
|CHROM=1
|dbSNPBuildID=129
|SSR=0
|SAO=1
|VP=0x050168000605000002110100
|GENEINFO=PEX10:5192
|GENE_NAME=PEX10
|GENE_ID=5192
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.2408679G>A
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_153818.1:c.373C>T; 602859.0003
|CLNSIG=5
|CLNCUI=C0282525
|CLNDBN=Peroxisome biogenesis disorder 6B
|Disease=Peroxisome biogenesis disorder 6B
|CLNACC=RCV000007174.1
|Tags=RV;PM;PMC;SLO;NSN;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|RS=61750434
|CLNDSDBID=CN159233:614871
}}

{{PMID Auto
|PMID=9683594
|Title=Identification of PEX10, the gene defective in complementation group 7 of the peroxisome-biogenesis disorders.
|OA=1
}}

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