Variant (rsID / SNP)
rs7903146
rs7903146 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TCF7L2. Location: chromosome 10, position 114,758,349. Clinical significance in the table: risk factor.
Reference-table entries
TCF7L2Risk factor
- Clinical significance (as recorded)
- risk factor
- Variant type
- single nucleotide variant
- Chromosome / position
- 10:114758349
- Cytoband
- 10q25.2
- HGVS
- NM_001367943.1(TCF7L2):c.450+33966C>T
- Allele change
- Silent
Associated conditions / phenotypes
Diabetes mellitus type 2, susceptibility to
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.