ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.164-8_164-3del

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
MVZ Medizinische Genetik Mainz RCV003984929 SCV004801044 uncertain significance Hereditary diffuse gastric adenocarcinoma 2023-07-06 criteria provided, single submitter clinical testing PM2_MOD, PP3

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