Variant (rsID / SNP)
rs111773256
rs111773256 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to STK11. Location: chromosome 19, position 1,228,260. Clinical significance in the table: Benign.
Reference-table entries
STK11Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 19:1228260
- Cytoband
- 19p13.3
- HGVS
- NM_000455.5(STK11):c.*685C>A
- Allele change
- Silent
Associated conditions / phenotypes
Peutz-Jeghers syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.