{{Rsnum
|rsid=104894616
|Chromosome=17
|Orientation=minus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=PEX12
|position=35576171
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PEX12
}}{{omim
|id=601758
|rsnum=104894616
|variant=0004
}}{{ClinVar
|rsid=104894616
|Reversed=1
|FwdREF=A
|FwdALT=T
|REF=T
|ALT=A
|RSPOS=33903190
|CHROM=17
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=PEX12:5193
|GENE_NAME=PEX12
|GENE_ID=5193
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000017.10:g.33903190T>A
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNACC=RCV000008215.1
|CLNDBN=Peroxisome biogenesis disorder 3A
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=CN159227:614859:912
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=601758.0004
|Disease=Peroxisome biogenesis disorder 3A
}}