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Variant (rsID / SNP)

rs766505270

CDH1

rs766505270 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CDH1. Location: chromosome 16, position 68,847,248. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

CDH1Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
16:68847248
Cytoband
16q22.1
HGVS
NM_004360.5(CDH1):c.1170C>T (p.Asn390=)
Allele change
Synonymous_N390N

Associated conditions / phenotypes

Hereditary cancer-predisposing syndrome|Hereditary diffuse gastric adenocarcinoma|Malignant tumor of breast

Public references

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