{{Rsnum
|rsid=80356714
|Chromosome=X
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=ABCB7
|position=75070433
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ABCB7
}}{{omim
|id=300135
|rsnum=80356714
|variant=0002
}}{{ClinVar
|rsid=80356714
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=74290268
|CHROM=X
|dbSNPBuildID=131
|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.74290268C>T
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1321; 300135.0002
|CLNSIG=5
|CLNCUI=C1845028; C1845028
|CLNDBN=Anemia sideroblastic and spinocerebellar ataxia
|Disease=Anemia sideroblastic and spinocerebellar ataxia
|CLNACC=RCV000012331.21
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1321:C1845028:301310:2802
}}{{PMID|11050011}} Human ABC7 transporter: gene structure and mutation causing X-linked sideroblastic anemia with ataxia with disruption of cytosolic iron-sulfur protein maturation.