ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.29144C>T (p.Ala9715Val)

dbSNP: rs533172128
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000382634 SCV000345127 uncertain significance not provided 2017-11-18 criteria provided, single submitter clinical testing
GeneDx RCV000382634 SCV001789486 likely benign not provided 2020-02-19 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV000382634 SCV004237400 uncertain significance not provided 2023-02-06 criteria provided, single submitter clinical testing

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