Variant (rsID / SNP)
rs876660765
rs876660765 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to APC. Location: chromosome 5, position 112,151,291. Clinical significance in the table: Pathogenic/Likely pathogenic.
Reference-table entries
APCPathogenic
- Clinical significance (as recorded)
- Pathogenic/Likely pathogenic
- Variant type
- single nucleotide variant
- Chromosome / position
- 5:112151291
- Cytoband
- 5q22.2
- HGVS
- NM_000038.6(APC):c.933+1G>A
- Allele change
- Silent
Associated conditions / phenotypes
Hereditary cancer-predisposing syndrome|Carcinoma of colon|Desmoid disease, hereditary|Hepatocellular carcinoma|Neoplasm of stomach|Familial adenomatous polyposis 1|Familial adenomatous polyposis 1
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.