{{Rsnum
|rsid=201777056
|Chromosome=14
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=ABCD4
|position=74292623
|Gene_s=ABCD4
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=14
|CLNACC=RCV000030859.2; RCV000059785.1
|CLNALLE=1
|CLNDBN=METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblJ TYPE; not provided
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=CN158715:614857:369955
|CLNHGVS=NC_000014.8:g.74759326T>C
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant; UniProtKB (variants)
|CLNSRCID=603214.0001; VAR_069097
|Disease=METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA; not provided
|FwdALT=C
|FwdREF=T
|GENEINFO=ABCD4:5826
|GENE_ID=5826
|GENE_NAME=ABCD4
|REF=T
|RSPOS=74759326
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;SLO;OTHERKG;LSD
|VC=SNV
|VP=0x050168000000000002100100
|WGT=0
|dbSNPBuildID=137
|rsid=201777056
}}{{PMID Auto
|PMID=22922874
|Title=Mutations in ABCD4 cause a new inborn error of vitamin B12 metabolism.
}}