Gene entry
ABCB7
ATP binding cassette subfamily B member 7
- Chromosome
- X
- Cytoband
- Xq13.3
- Variants (rsID)
- 20
ABCB7 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome X (region Xq13.3). Its official name is “ATP binding cassette subfamily B member 7”. The reference table lists 20 variants (rsID) for this gene.
Clinically classified variants
4 reference-table entries with clinical significance.
- rs1340989Benignsingle nucleotide variantSideroblastic Anemia and Ataxia
- rs151288786Benignsingle nucleotide variantX-linked sideroblastic anemia with ataxia
- rs61323727Conflicting interpretationssingle nucleotide variantSideroblastic Anemia and Ataxia
- rs1133577Likely pathogenicsingle nucleotide variant
Other listed variants
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.