Gene entry
TCF7L2
transcription factor 7 like 2
- Chromosome
- 10
- Cytoband
- 10q25.2-q25.3
- Variants (rsID)
- 82
TCF7L2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 10 (region 10q25.2-q25.3). Its official name is “transcription factor 7 like 2”. The reference table lists 82 variants (rsID) for this gene.
Clinically classified variants
3 reference-table entries with clinical significance.
- rs7904519Benignsingle nucleotide variant
- rs12255372Risk factorsingle nucleotide variantDiabetes mellitus type 2, susceptibility to
- rs7903146Risk factorsingle nucleotide variantDiabetes mellitus type 2, susceptibility to
Other listed variants
- rs290481
- rs290487
- rs1225404
- rs1362943
- rs3814570
- rs4073288
- rs4132670
- rs4277044
- rs4506565
- rs4575195
- rs4917644
- rs4917645
- rs4918791
- rs4918792
- rs6585196
- rs6585206
- rs7074440
- rs7076754
- rs7079711
- rs7085532
- rs7089262
- rs7100388
- rs7901275
- rs7901695
- rs7917983
- rs7919152
- rs7919409
- rs10787476
- rs10787479
- rs10885401
- rs10885417
- rs11196172
- rs11196212
- rs11196229
- rs11592706
- rs12243326
- rs12244851
- rs12571590
- rs12762233
- rs12772424
- rs17130188
- rs17747324
- rs34210369
- rs34855922
- rs34872471
- rs35010564
- rs35011184
- rs55878518
- rs56087297
- rs56135213
- rs57255539
- rs57543781
- rs61872787
- rs61875103
- rs61875105
- rs61875120
- rs72641339
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.