ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.87354del (p.Ala29119fs)

dbSNP: rs1559262463
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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 RCV000768873 SCV000900246 likely pathogenic Cardiomyopathy 2016-02-26 criteria provided, single submitter clinical testing

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