ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.34453+6del

gnomAD frequency: 0.00001  dbSNP: rs764521300
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001559596 SCV001781859 likely benign not provided 2020-05-12 criteria provided, single submitter clinical testing
CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario RCV003150444 SCV003838022 uncertain significance Cardiomyopathy 2022-03-09 criteria provided, single submitter clinical testing

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