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Variant (rsID / SNP)

rs35572355

CDH1

rs35572355 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CDH1. Location: chromosome 16, position 68,867,247. Clinical significance in the table: Benign.

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Reference-table entries

CDH1Benign
Clinical significance (as recorded)
Benign
Variant type
single nucleotide variant
Chromosome / position
16:68867247
Cytoband
16q22.1
HGVS
NM_004360.5(CDH1):c.2494G>A (p.Val832Met)
Allele change
Missense_V832M

Associated conditions / phenotypes

Hereditary diffuse gastric adenocarcinoma|Hereditary cancer-predisposing syndrome|Neoplasm of stomach|Hereditary breast ovarian cancer syndrome

Public references

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