ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.68357del (p.Asn22786fs)

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Total submissions: 2
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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 RCV003150632 SCV003837979 likely pathogenic Cardiomyopathy 2022-04-08 criteria provided, single submitter clinical testing
Lildballe Lab, Aarhus University Hospital RCV004775354 SCV005200591 likely pathogenic Primary dilated cardiomyopathy 2024-03-01 criteria provided, single submitter research PVS1(vs), PM2(sup)

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