{{Rsnum
|rsid=72554634
|Chromosome=X
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=ABCB7
|position=75071516
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ABCB7
}}{{omim
|id=300135
|rsnum=72554634
|variant=0001
}}

{{ClinVar
|rsid=72554634
|Reversed=1
|FwdREF=T
|FwdALT=A,G
|REF=A
|ALT=C,T
|RSPOS=74291351
|CHROM=X
|dbSNPBuildID=130
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=ABCB7:22
|GENE_NAME=ABCB7
|GENE_ID=22
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.74291351A>C
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1321; 300135.0001
|CLNSIG=5
|CLNCUI=C1845028; C1845028
|CLNDBN=Anemia sideroblastic and spinocerebellar ataxia
|Disease=Anemia sideroblastic and spinocerebellar ataxia
|CLNACC=RCV000012330.23
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1321:C1845028:301310:2802
}}

{{PMID|10196363}} Mutation of a putative mitochondrial iron transporter gene (ABC7) in X-linked sideroblastic anemia and ataxia (XLSA/A).

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