{{Rsnum
|rsid=193922098
|Chromosome=X
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=ABCD1
|position=153726104
|Gene_s=ABCD1,BCAP31
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=193922098
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=152991559
|CHROM=X
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050068000000000002100100
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.152991559C>T
|CLNSRC=Correlagen
|CLNORIGIN=1
|CLNSIG=4
|CLNDBN=Adrenoleukodystrophy
|Disease=Adrenoleukodystrophy
|Tags=PM;PMC;OTHERKG;LSD
|CLNACC=RCV000029290.1
|CLNDSDB=GeneReviews:MedGen:OMIM:SNOMED_CT
|CLNDSDBID=NBK1315:C0162309:300100:65389002
|GENEINFO=BCAP31:10134; ABCD1:215
|GENE_ID=10134; 215
|GENE_NAME=BCAP31; ABCD1
}}{{PMID Auto
|PMID=11748843
|Title=ABCD1 mutations and the X-linked adrenoleukodystrophy mutation database: role in diagnosis and clinical correlations.
}}

{{PMID Auto
|PMID=15811009
|Title=X-linked adrenoleukodystrophy in Spain. Identification of 26 novel mutations in the ABCD1 gene in 80 patients. Improvement of genetic counseling in 162 relative females.
}}