ClinVar Miner

Submissions for variant NM_003803.3(MYOM1):c.3453T>A (p.Asp1151Glu) (rs143879853)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000227310 SCV000288001 benign Hypertrophic cardiomyopathy 2017-12-18 criteria provided, single submitter clinical testing
Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine RCV000215868 SCV000269359 benign not specified 2014-11-24 criteria provided, single submitter clinical testing Asp1151Glu in exon 23 of MYOM1: This variant is not expected to have clinical si gnificance because it has been identified in 1.8% (67/3808) of African American chromosomes from a broad population by the NHLBI Exome Sequencing Project (http: //evs.gs.washington.edu/EVS; dbSNP rs143879853).

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