ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.1937-25C>A

gnomAD frequency: 0.00030  dbSNP: rs201760019
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV002269067 SCV002551787 likely benign not specified 2025-03-04 criteria provided, single submitter clinical testing
European Reference Network on Genetic Tumour Risk Syndromes (ERN-GENTURIS), i3s - Instituto de Investigação e Inovação em Saúde, University of Porto RCV003229634 SCV003926876 uncertain significance Hereditary diffuse gastric adenocarcinoma 2022-08-01 criteria provided, single submitter clinical testing BS2_Supporting (PMID: 30311375)

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