Variant (rsID / SNP)

rs587781919

rs587781919 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CDH1. Location: chromosome 16, position 68,835,797. Clinical significance in the table: Uncertain significance.

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Reference-table entries

CDH1Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 16:68835797
Cytoband: 16q22.1
HGVS: NM_004360.5(CDH1):c.387+1G>A
Allele change: Silent

Associated conditions / phenotypes

Hereditary cancer-predisposing syndrome|Hereditary diffuse gastric adenocarcinoma

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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