{{Rsnum
|rsid=61752138
|Chromosome=12
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=PEX5
|position=7209700
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PEX5
}}{{omim
|id=600414
|rsnum=61752138
|variant=0001
}}

{{ClinVar
|rsid=61752138
|Reversed=0
|FwdREF=T
|FwdALT=G
|REF=T
|ALT=G
|RSPOS=7362296
|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.7362296T>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600414.0001
|CLNSIG=5
|CLNCUI=C0282525
|CLNDBN=Neonatal adrenoleucodystrophy
|Disease=Neonatal adrenoleucodystrophy
|CLNACC=RCV000009714.1
|Tags=PM;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:SNOMED_CT
|CLNDSDBID=NBK1448:C0282525:202370:238061001
}}

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