{{Rsnum
|rsid=61752112
|Chromosome=17
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PEX12
|position=35575913
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PEX12
}}{{omim
|id=601758
|rsnum=61752112
|variant=0010
}}

{{ClinVar
|rsid=61752112
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=33902932
|CHROM=17
|dbSNPBuildID=129
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=PEX12:5193
|GENE_NAME=PEX12
|GENE_ID=5193
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000017.10:g.33902932G>A
|CLNORIGIN=0
|CLNSIG=5
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000008221.1
|CLNDBN=PEROXISOMAL BIOGENESIS DISORDER 3B
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=601758.0010
|Disease=PEROXISOMAL BIOGENESIS DISORDER 3B
}}

{{PMID Auto
|PMID=15241794
|Title=Identification of the molecular defect in patients with peroxisomal mosaicism using a novel method involving culturing of cells at 40 degrees C: implications for other inborn errors of metabolism.
}}

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