Variant (rsID / SNP)
rs786203477
rs786203477 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PTEN. Location: chromosome 10, position 89,653,783. Clinical significance in the table: Pathogenic.
Reference-table entries
PTENPathogenic
- Clinical significance (as recorded)
- Pathogenic
- Variant type
- Insertion
- Chromosome / position
- 10:89653783
- Cytoband
- 10q23.31
- HGVS
- NM_000314.8(PTEN):c.81_82insCT (p.Ile28fs)
Associated conditions / phenotypes
Hereditary cancer-predisposing syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.