{{Rsnum
|rsid=74315506
|Chromosome=22
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PEX26
|position=18078378
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PEX26
}}{{omim
|id=608666
|rsnum=74315506
|variant=0005
}}{{ClinVar
|rsid=74315506
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=18561144
|CHROM=22
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050160000000000002110100
|GENEINFO=PEX26:55670
|GENE_NAME=PEX26
|GENE_ID=55670
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000022.10:g.18561144T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=608666.0005
|CLNSIG=5
|CLNCUI=C0282527
|CLNDBN=Peroxisome biogenesis disorder 7B
|Disease=Peroxisome biogenesis disorder 7B
|CLNACC=RCV000002239.1
|Tags=PM;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=CN159235:614873
}}