ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.2440-13C>A

dbSNP: rs1567517555
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002185254 SCV002352137 likely benign Hereditary diffuse gastric adenocarcinoma 2021-04-30 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV005232807 SCV005872408 likely benign not specified 2025-03-04 criteria provided, single submitter clinical testing Classification criteria: BP4

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