ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.101001T>A (p.Tyr33667Ter)

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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 RCV003487200 SCV004240214 likely pathogenic Cardiomyopathy 2023-01-31 criteria provided, single submitter clinical testing

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