ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.86003T>A (p.Ile28668Lys) (rs374022393)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000253568 SCV000318150 uncertain significance Cardiovascular phenotype 2013-01-11 criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV000516316 SCV000616163 uncertain significance not specified 2017-04-21 criteria provided, single submitter clinical testing
Ambry Genetics RCV000624511 SCV000742387 uncertain significance Inborn genetic diseases 2017-04-06 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: UNCERTAIN: Alteration(s) of Uncertain Clinical Significance Detected

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