ClinVar Miner

Submissions for variant NM_003803.3(MYOM1):c.4069+4A>C (rs80328493)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000234373 SCV000288003 benign Hypertrophic cardiomyopathy 2017-12-28 criteria provided, single submitter clinical testing
Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine RCV000611253 SCV000711566 benign not specified 2014-11-24 criteria provided, single submitter clinical testing 4069+4A>C in intron 28 of MYOM1: This variant is not expected to have clinical s ignificance because it has been identified in 2.8% (99/3580) of African American chromosomes from a broad population by the NHLBI Exome Sequencing Project (http ://; dbSNP rs80328493).

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