ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.5759T>A (p.Val1920Glu)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Molecular Genetics, Labor Dr. Heidrich & Kollegen MVZ GmbH RCV004719055 SCV005324754 uncertain significance not provided 2024-02-29 no assertion criteria provided clinical testing

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