ClinVar Miner

Submissions for variant NM_001145809.2(MYH14):c.4255C>T (p.Arg1419Trp) (rs115019972)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine, Partners HealthCare Personalized Medicine RCV000151193 SCV000199024 benign not specified 2012-05-07 criteria provided, single submitter clinical testing Arg1419Trp in Exon 32 of MYH14: This variant is not expected to have clinical si gnificance because it has been identified in 1.0% (26/2612) of African American chromosomes from a broad population by the NHLBI Exome Sequencing Project (http: //evs.gs.washington.edu/EVS; dbSNP rs115019972).
Invitae RCV000884155 SCV001027511 benign not provided 2019-12-31 criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV000884155 SCV001144629 benign not provided 2019-02-27 criteria provided, single submitter clinical testing

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