ClinVar Miner

Submissions for variant NM_133379.5(TTN):c.7057+2dup (rs765019023)

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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 RCV000172463 SCV000055102 uncertain significance not provided 2013-06-24 criteria provided, single submitter research
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000172463 SCV000859441 uncertain significance not provided 2018-01-30 criteria provided, single submitter clinical testing
Blueprint Genetics RCV000172463 SCV000928192 likely pathogenic not provided 2019-01-29 criteria provided, single submitter clinical testing

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