ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.33754C>A (p.Pro11252Thr)

dbSNP: rs886055283
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000504045 SCV000597698 uncertain significance not specified 2016-11-22 criteria provided, single submitter clinical testing
Eurofins Ntd Llc (ga) RCV000734713 SCV000862877 uncertain significance not provided 2018-08-17 criteria provided, single submitter clinical testing
GeneDx RCV000734713 SCV001990844 uncertain significance not provided 2019-03-29 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV000734713 SCV003824127 uncertain significance not provided 2020-08-27 criteria provided, single submitter clinical testing

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