{{Rsnum
|rsid=104893661
|Chromosome=2
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=PEX13
|position=61032028
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PEX13
}}{{omim
|id=601789
|rsnum=104893661
|variant=0001
}}{{ClinVar
|rsid=104893661
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=61259163
|CHROM=2
|dbSNPBuildID=132
|SSR=0
|SAO=0
|VP=0x050060000000000002110100
|GENEINFO=PEX13:5194
|GENE_NAME=PEX13
|GENE_ID=5194
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.61259163G>A
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=601789.0001
|CLNSIG=5
|CLNCUI=C0043459
|CLNDBN=Peroxisome biogenesis disorder 11A
|Disease=Peroxisome biogenesis disorder 11A
|CLNACC=RCV000008142.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=CN159240:614883:912
}}