ClinVar Miner

Submissions for variant NM_133379.5(TTN):c.11757C>G (p.Phe3919Leu)

gnomAD frequency: 0.00002  dbSNP: rs369074426
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine RCV000041008 SCV000064699 uncertain significance not specified 2013-10-03 criteria provided, single submitter clinical testing

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