Variant (rsID / SNP)
rs587782172
rs587782172 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MSH6. Location: chromosome 2, position 48,023,201. Clinical significance in the table: Pathogenic.
Reference-table entries
MSH6Pathogenic
- Clinical significance (as recorded)
- Pathogenic
- Variant type
- Deletion
- Chromosome / position
- 2:48023201
- Cytoband
- 2p16.3
- HGVS
- NM_000179.3(MSH6):c.626_627+15del
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.