ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.18199A>G (p.Thr6067Ala)

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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 RCV005240123 SCV005887024 uncertain significance not specified 2025-01-27 criteria provided, single submitter clinical testing

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