ClinVar Miner

Submissions for variant NM_003803.4(MYOM1):c.*10C>T (rs876657915)

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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 RCV000214769 SCV000272162 uncertain significance not specified 2015-11-11 criteria provided, single submitter clinical testing The c.*10C>T variant in MYOM1 has not been previously reported in individuals wi th cardiomyopathy and was absent from large population studies. Computational pr ediction tools and conservation analysis are limited or unavailable for this var iant. In summary, the clinical significance of the c.*10C>T variant is uncertain .

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