Variant (rsID / SNP)
rs6899169
rs6899169 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to APC. Location: chromosome 5, position 112,171,097. Clinical significance in the table: Benign.
Reference-table entries
APCBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 5:112171097
- Cytoband
- 5q22.2
- HGVS
- NM_000038.6(APC):c.1958+235A>G
- Allele change
- Silent
Associated conditions / phenotypes
Familial colorectal cancer
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.