ClinVar Miner

Submissions for variant NM_003803.3(MYOM1):c.93G>A (p.Arg31=) (rs876657536)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000629101 SCV000750014 likely benign Hypertrophic cardiomyopathy 2017-12-05 criteria provided, single submitter clinical testing
Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine RCV000221621 SCV000270574 likely benign not specified 2015-07-02 criteria provided, single submitter clinical testing p.Arg31Arg in exon 2 of MYOM1: This variant is not expected to have clinical sig nificance because it does not alter an amino acid residue and is not located wit hin the splice consensus sequence.

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