Gene entry
ITFG1
integrin alpha FG-GAP repeat containing 1
- Chromosome
- 16
- Cytoband
- 16q12.1
- Variants (rsID)
- 20
ITFG1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 16 (region 16q12.1). Its official name is “integrin alpha FG-GAP repeat containing 1”. The reference table lists 20 variants (rsID) for this gene.
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.
