ClinVar Miner

Submissions for variant NM_000364.4(TNNT2):c.313A>G (p.Met105Val) (rs397516458)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine RCV000036577 SCV000060232 uncertain significance not specified 2009-03-03 no assertion criteria provided clinical testing

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