Gene entry
CBLIF
cobalamin binding intrinsic factor
- Chromosome
- 11
- Cytoband
- 11q12.1
- Variants (rsID)
- 2
CBLIF is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 11 (region 11q12.1). Its official name is “cobalamin binding intrinsic factor”. The reference table lists 2 variants (rsID) for this gene.
Clinically classified variants
2 reference-table entries with clinical significance.
- rs150884181Benignsingle nucleotide variantHereditary intrinsic factor deficiency
- rs35211634Benignsingle nucleotide variantIntrinsic factor deficiency, congenital, susceptibility to|Hereditary intrinsic factor deficiency
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.