ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.76776C>G (p.Ala25592=)

dbSNP: rs2468402596
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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 RCV003150706 SCV003838553 likely benign Cardiomyopathy 2021-11-01 criteria provided, single submitter clinical testing

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