ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.48361C>G (p.Gln16121Glu)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV003317976 SCV004020319 uncertain significance not specified 2023-06-10 criteria provided, single submitter clinical testing

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