ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.50344C>G (p.Pro16782Ala)

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Total submissions: 2
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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 RCV003404941 SCV004122654 uncertain significance not specified 2023-10-09 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV003429120 SCV004152400 uncertain significance not provided 2023-03-01 criteria provided, single submitter clinical testing TTN: PM2

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