ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.83388T>A (p.Ala27796=)

dbSNP: rs763818465
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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 RCV000769923 SCV000901349 likely benign Cardiomyopathy 2017-01-09 criteria provided, single submitter clinical testing

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