ClinVar Miner

Submissions for variant NM_003803.3(MYOM1):c.-9G>A (rs1662315)

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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 RCV000220381 SCV000269380 benign not specified 2014-11-24 criteria provided, single submitter clinical testing -9G>A in exon 2 of MYOM1: This variant is not expected to have clinical signific ance because it has been identified in 27.9% (1141/4096) of African American chr omosomes from a broad population by the NHLBI Exome Sequencing Project (http://e vs.gs.washington.edu/EVS; dbSNP rs1662315).

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