ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.24595C>T (p.Pro8199Ser)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV003994874 SCV004813389 uncertain significance not specified 2024-02-04 criteria provided, single submitter clinical testing

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