Gene entry
TF
transferrin
- Chromosome
- 3
- Cytoband
- 3q22.1
- Variants (rsID)
- 48
TF is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 3 (region 3q22.1). Its official name is “transferrin”. The reference table lists 48 variants (rsID) for this gene.
Clinically classified variants
7 reference-table entries with clinical significance.
- rs1049296Benignsingle nucleotide variantAlzheimer disease, susceptibility to|Transferrin variant c1/c2|Atransferrinemia
- rs1799852Benignsingle nucleotide variantAtransferrinemia
- rs1799899Benignsingle nucleotide variantIron deficiency anemia|Atransferrinemia
- rs41295774Benignsingle nucleotide variantTransferrin variant chi|Atransferrinemia
- rs121918677Conflicting interpretationssingle nucleotide variantTransferrin variant b2|Atransferrinemia
- rs121918680Pathogenicsingle nucleotide variantAtransferrinemia
- rs41296598Uncertain significancesingle nucleotide variantAtransferrinemia
Other listed variants
- rs1800277
- rs1830084
- rs1880669
- rs2589268
- rs3811647
- rs4241356
- rs4419374
- rs4459901
- rs4854742
- rs8177178
- rs8177189
- rs8177191
- rs8177197
- rs8177217
- rs8177235
- rs8177240
- rs8177253
- rs8177271
- rs9820225
- rs9843728
- rs12638146
- rs13325440
- rs28451696
- rs41295792
- rs56264440
- rs57942494
- rs62280567
- rs62280570
- rs74639761
- rs76288814
- rs77533208
- rs77596238
- rs79097140
- rs79351379
- rs114635016
- rs114979188
- rs144143295
- rs148759181
- rs150280363
- rs200493748
- rs371228865
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.