ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.93431G>A (p.Arg31144Gln)

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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 RCV003388507 SCV004100124 uncertain significance not specified 2023-09-25 criteria provided, single submitter clinical testing

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