Variant (rsID / SNP)
rs141769154
rs141769154 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TEK. Location: chromosome 9, position 27,202,986. Clinical significance in the table: Uncertain significance.
Reference-table entries
TEKUncertain significance
- Clinical significance (as recorded)
- Uncertain significance
- Variant type
- single nucleotide variant
- Chromosome / position
- 9:27202986
- Cytoband
- 9p21.2
- HGVS
- NM_000459.5(TEK):c.2078C>T (p.Thr693Ile)
- Allele change
- Missense_T650I
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.