ClinVar Miner

Submissions for variant NM_002471.3(MYH6):c.4134G>A (p.Glu1378=) (rs1555333539)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000620584 SCV000736157 likely benign Cardiovascular phenotype 2016-07-14 criteria provided, single submitter clinical testing Synonymous alterations with insufficient evidence to classify as benign
Integrated Genetics/Laboratory Corporation of America RCV001192375 SCV001360443 likely benign not specified 2019-08-16 criteria provided, single submitter clinical testing

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