ClinVar Miner

Submissions for variant NM_004360.5:c.2164_2439del

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Department of Clinical Genetics, Copenhagen University Hospital, Rigshospitalet RCV005055485 SCV005689634 likely pathogenic Hereditary diffuse gastric adenocarcinoma 2025-02-04 criteria provided, single submitter clinical testing PVS1_Strong; PM2_SUP; PP3

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