ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.65725G>T (p.Gly21909Cys)

gnomAD frequency: 0.00001  dbSNP: rs878898044
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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 RCV003487158 SCV004240063 likely benign Cardiomyopathy 2022-09-02 criteria provided, single submitter clinical testing

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