ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.101331A>C (p.Ser33777=)

dbSNP: rs2468569821
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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 RCV003150624 SCV003837952 likely benign Cardiomyopathy 2022-02-16 criteria provided, single submitter clinical testing

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