ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.16549T>G (p.Ser5517Ala)

dbSNP: rs200520316
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Biesecker Lab/Clinical Genomics Section, National Institutes of Health RCV000172404 SCV000055067 uncertain significance not provided 2013-06-24 criteria provided, single submitter research
Genetic Services Laboratory, University of Chicago RCV000192411 SCV000249234 uncertain significance not specified 2014-11-04 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV000172404 SCV003819748 uncertain significance not provided 2019-10-30 criteria provided, single submitter clinical testing

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