{{Rsnum
|rsid=61752137
|Chromosome=12
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PEX5
|position=7208554
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PEX5
}}{{omim
|id=600414
|rsnum=61752137
|variant=0002
}}

{{ClinVar
|rsid=61752137
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=7361150
|CHROM=12
|dbSNPBuildID=129
|SSR=0
|SAO=1
|VP=0x050360000000000002110100
|GENEINFO=PEX5:5830
|GENE_NAME=PEX5
|GENE_ID=5830
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000012.11:g.7361150C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=600414.0002
|CLNSIG=5
|CLNCUI=C0043459
|CLNDBN=Peroxisome biogenesis disorder 2A
|Disease=Peroxisome biogenesis disorder 2A
|CLNACC=RCV000009715.3
|Tags=PM;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:OMIM:Orphanet
|CLNDSDBID=C1859228:214100:214110:912
}}

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