Variant (rsID / SNP)
rs142822590
rs142822590 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CDH1. Location: chromosome 16, position 68,845,646. Clinical significance in the table: Benign.
Reference-table entries
CDH1Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 16:68845646
- Cytoband
- 16q22.1
- HGVS
- NM_004360.5(CDH1):c.892G>A (p.Ala298Thr)
- Allele change
- Missense_A298T
Associated conditions / phenotypes
Hereditary diffuse gastric adenocarcinoma|Hereditary cancer-predisposing syndrome|Neoplasm of stomach|Colon cancer|Malignant tumor of breast|Breast and/or ovarian cancer
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.