ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.24677C>G (p.Thr8226Ser)

dbSNP: rs1391244402
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Athena Diagnostics RCV000518593 SCV000616031 uncertain significance not specified 2016-11-11 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004691831 SCV005188152 uncertain significance not provided criteria provided, single submitter not provided

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