Variant (rsID / SNP)
rs1800931
rs1800931 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MSH6. Location: chromosome 2, position 48,018,030. Clinical significance in the table: Benign.
Reference-table entries
MSH6Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 2:48018030
- Cytoband
- 2p16.3
- HGVS
- NM_000179.3(MSH6):c.261-36A>G
- Allele change
- Silent
Associated conditions / phenotypes
Lynch syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.