ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.19541G>T (p.Trp6514Leu)

gnomAD frequency: 0.00006  dbSNP: rs760007747
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000381097 SCV000334181 uncertain significance not provided 2015-08-20 criteria provided, single submitter clinical testing
GeneDx RCV000381097 SCV001794504 likely benign not provided 2020-12-18 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV002265723 SCV002547649 uncertain significance not specified 2022-05-02 criteria provided, single submitter clinical testing
Revvity Omics, Revvity Omics RCV000381097 SCV003819015 uncertain significance not provided 2023-12-05 criteria provided, single submitter clinical testing

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