Gene entry
FTL
ferritin light chain
- Chromosome
- 19
- Cytoband
- 19q13.33
- Variants (rsID)
- 3
FTL is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 19 (region 19q13.33). Its official name is “ferritin light chain”. The reference table lists 3 variants (rsID) for this gene.
Clinically classified variants
2 reference-table entries with clinical significance.
- rs201241191Benignsingle nucleotide variantsporadic abdominal aortic aneurysm|Neuroferritinopathy|Hereditary hyperferritinemia with congenital cataracts
- rs5452Conflicting interpretationssingle nucleotide variantHereditary hyperferritinemia with congenital cataracts|Neuroferritinopathy|Glycogen storage disease due to muscle and heart glycogen synthase deficiency
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.