Variant (rsID / SNP)
rs200756935
rs200756935 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to APC. Location: chromosome 5, position 112,178,327. Clinical significance in the table: Conflicting interpretations of pathogenicity.
Reference-table entries
APCConflicting interpretations
- Clinical significance (as recorded)
- Conflicting interpretations of pathogenicity
- Variant type
- single nucleotide variant
- Chromosome / position
- 5:112178327
- Cytoband
- 5q22.2
- HGVS
- NM_000038.6(APC):c.7036C>T (p.Pro2346Ser)
- Allele change
- Missense_P2346S
Associated conditions / phenotypes
Hereditary cancer-predisposing syndrome|Hepatocellular carcinoma|Familial adenomatous polyposis 1|Neoplasm of stomach|Desmoid disease, hereditary|Carcinoma of colon|Familial adenomatous polyposis 1|APC-Associated Polyposis Disorders|Colorectal cancer|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.