ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.41002CCT[1] (p.Pro13669del)

dbSNP: rs747793660
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Athena Diagnostics RCV001289376 SCV001477142 uncertain significance not provided 2020-06-03 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV001289376 SCV003819667 uncertain significance not provided 2019-08-29 criteria provided, single submitter clinical testing
New York Genome Center RCV003336372 SCV004046528 uncertain significance Dilated cardiomyopathy 1G; Hypertrophic cardiomyopathy 9 2023-02-24 criteria provided, single submitter clinical testing

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