ClinVar Miner

Submissions for variant NM_002878.4(RAD51D):c.565_576+25del

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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 RCV005055473 SCV005689572 likely pathogenic Hereditary cancer-predisposing syndrome 2025-02-04 criteria provided, single submitter clinical testing PVS1; PM2_SUP

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