{{Rsnum
|rsid = 28936698
|Gene = PEX12
|Orientation=minus
|ReferenceAllele=A
|MissenseAllele=T
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Chromosome=17
|position=35577445
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PEX12
}}{{omim
|desc=PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP 3
|id=601758
|rsnum=28936698
|variant=0009
}}

{{ClinVar
|rsid=28936698
|Reversed=1
|FwdREF=A
|FwdALT=T
|REF=T
|ALT=A
|RSPOS=33904464
|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.33904464T>A
|CLNORIGIN=0
|CLNSIG=5
|Tags=RV;PM;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000008220.1
|CLNDBN=PEROXISOMAL BIOGENESIS DISORDER 3B
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=601758.0009
|Disease=PEROXISOMAL BIOGENESIS DISORDER 3B
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}