ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.29191T>A (p.Trp9731Arg)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario RCV003487130 SCV004239877 likely benign Cardiomyopathy 2023-04-21 criteria provided, single submitter clinical testing

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