{{Rsnum
|rsid=61752103
|Chromosome=17
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PEX12
|position=35577180
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PEX12
}}{{omim
|id=601758
|rsnum=61752103
|variant=0005
}}

{{ClinVar
|rsid=61752103
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=33904199
|CHROM=17
|dbSNPBuildID=129
|SSR=0
|SAO=1
|VP=0x050160000000000002110100
|GENEINFO=PEX12:5193
|GENE_NAME=PEX12
|GENE_ID=5193
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000017.10:g.33904199G>A
|CLNORIGIN=0
|CLNSIG=5
|Tags=RV;PM;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000008216.1; RCV000032926.1
|CLNDBN=Peroxisome biogenesis disorder 3A; PEROXISOMAL BIOGENESIS DISORDER 3B
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=CN159227:614859:912
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=601758.0005
|Disease=Peroxisome biogenesis disorder 3A; PEROXISOMAL BIOGENESIS DISORDER 3B
}}

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