ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.63254G>A (p.Trp21085Ter)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Clinical Genetics Laboratory, Skane University Hospital Lund RCV004698208 SCV005198908 likely pathogenic not provided 2023-05-24 criteria provided, single submitter clinical testing

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