ClinVar Miner

Submissions for variant NM_003803.3(MYOM1):c.1023-14G>A (rs372359086)

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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 RCV000221210 SCV000270554 likely benign not specified 2015-04-03 criteria provided, single submitter clinical testing c.1023-14G>A in intron 6 of MYOM1: This variant is not expected to have clinical significance because it has been identified in 0.9% (147/16350) of South Asian chromosomes by the Exome Aggregation Consortium (ExAC, http://exac.broadinstitut e.org; dbSNP rs372359086).

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