ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.100659C>A (p.His33553Gln)

dbSNP: rs746903660
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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 RCV001170521 SCV001333104 uncertain significance Cardiomyopathy 2017-11-21 criteria provided, single submitter clinical testing

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