Variant (rsID / SNP)
rs863225415
rs863225415 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MSH6. Location: chromosome 2, position 48,033,643. Clinical significance in the table: Benign.
Reference-table entries
MSH6Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- Duplication
- Chromosome / position
- 2:48033643
- Cytoband
- 2p16.3
- HGVS
- NM_000179.3(MSH6):c.3854dup (p.Leu1286fs)
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.