ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.64671G>A (p.Met21557Ile)

dbSNP: rs786205387
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Total submissions: 2
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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 RCV000172285 SCV000054960 uncertain significance not provided 2013-06-24 criteria provided, single submitter research
Revvity Omics, Revvity Omics RCV000172285 SCV003821717 uncertain significance not provided 2021-07-26 criteria provided, single submitter clinical testing

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