Variant (rsID / SNP)

rs370864592

rs370864592 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CDH1. Location: chromosome 16, position 68,849,506. 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: 16:68849506
Cytoband: 16q22.1
HGVS: NM_004360.5(CDH1):c.1409C>T (p.Thr470Ile)
Allele change: Missense_T470I

Associated conditions / phenotypes

Hereditary cancer-predisposing syndrome|Hereditary diffuse gastric adenocarcinoma|Hereditary breast ovarian cancer syndrome

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.