ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.76373del (p.Pro25458fs)

dbSNP: rs869025553
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Blueprint Genetics RCV000788789 SCV000928032 pathogenic not provided 2018-11-02 criteria provided, single submitter clinical testing
Clinical Genetics Laboratory, Skane University Hospital Lund RCV000788789 SCV005198904 likely pathogenic not provided 2022-05-27 criteria provided, single submitter clinical testing

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