ClinVar Miner

Submissions for variant NM_001110556.2(FLNA):c.4106C>T (p.Thr1369Ile) (rs376774130)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000729237 SCV000639786 likely benign not provided 2018-11-26 criteria provided, single submitter clinical testing
Ambry Genetics RCV000622238 SCV000739115 uncertain significance Cardiovascular phenotype 2017-07-28 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: Insufficient evidence
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000729237 SCV000856880 uncertain significance not provided 2017-09-27 criteria provided, single submitter clinical testing

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