ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.18927C>G (p.Ala6309=)

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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 RCV003150737 SCV003838660 likely benign Cardiomyopathy 2021-07-21 criteria provided, single submitter clinical testing

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