ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.7439del (p.Tyr2479_Leu2480insTer)

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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 RCV004698219 SCV005198935 likely pathogenic not provided 2023-06-15 criteria provided, single submitter clinical testing

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