{{Rsnum
|rsid=61752116
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PEX14
|position=10624405
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PEX14
}}{{omim
|id=601791
|rsnum=61752116
|variant=0001
}}

{{ClinVar
|rsid=61752116
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=10624405
|CHROM=1
|dbSNPBuildID=129
|SSR=0
|SAO=1
|VP=0x050160000605000002110100
|GENEINFO=PEX14:5195
|GENE_NAME=PEX14
|GENE_ID=5195
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.10624405C>T
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_004565.2:c.553C>T; 601791.0001
|CLNSIG=5
|CLNCUI=C0043459
|CLNDBN=Peroxisome biogenesis disorder 13A
|Disease=Peroxisome biogenesis disorder 13A
|CLNACC=RCV000008140.2
|Tags=PM;SLO;NSN;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=CN159243:614887:ORPHA912
}}

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