Variant (rsID / SNP)

rs786202151

rs786202151 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CDH1. Location: chromosome 16, position 68,835,611. Clinical significance in the table: Pathogenic.

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Reference-table entries

CDH1Pathogenic

Clinical significance (as recorded): Pathogenic
Variant type: Deletion
Chromosome / position: 16:68835611
Cytoband: 16q22.1
HGVS: NM_004360.5(CDH1):c.202del (p.Tyr68fs)

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.