ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.61411del (p.Leu20471fs)

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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 RCV004698209 SCV005198909 pathogenic not provided 2022-09-28 criteria provided, single submitter clinical testing

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