ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.2295+45C>T

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
European Reference Network on Genetic Tumour Risk Syndromes (ERN-GENTURIS), i3s - Instituto de Investigação e Inovação em Saúde, University of Porto RCV003229730 SCV003926917 uncertain significance Hereditary diffuse gastric adenocarcinoma 2022-08-01 criteria provided, single submitter clinical testing Not applicable criteria (PMID: 30311375)
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV003321984 SCV004026654 likely benign not specified 2023-08-15 criteria provided, single submitter clinical testing

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