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Variant (rsID / SNP)

rs587780786

CDH1

rs587780786 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CDH1. Location: chromosome 16, position 68,853,306. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

CDH1Benign
Clinical significance (as recorded)
Benign/Likely benign
Variant type
single nucleotide variant
Chromosome / position
16:68853306
Cytoband
16q22.1
HGVS
NM_004360.5(CDH1):c.1689C>T (p.Ala563=)
Allele change
Synonymous_A563A

Associated conditions / phenotypes

Hereditary diffuse gastric adenocarcinoma|Hereditary cancer-predisposing syndrome

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.