{{Rsnum
|rsid=61752115
|Chromosome=2
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PEX13
|position=61048535
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PEX13
}}{{omim
|id=601789
|rsnum=61752115
|variant=0002
}}

{{ClinVar
|rsid=61752115
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=61275670
|CHROM=2
|dbSNPBuildID=129
|SSR=0
|SAO=1
|VP=0x050360000000000002110100
|GENEINFO=PEX13:5194
|GENE_NAME=PEX13
|GENE_ID=5194
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.61275670T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=601789.0002
|CLNSIG=5
|CLNCUI=C0282525
|CLNDBN=Peroxisome biogenesis disorder 11B
|Disease=Peroxisome biogenesis disorder 11B
|CLNACC=RCV000008143.1
|Tags=PM;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=CN159241:614885
}}

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