ClinVar Miner

Submissions for variant NM_002471.3(MYH6):c.736-9C>T (rs748594445)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine RCV000221718 SCV000270454 likely benign not specified 2014-12-18 criteria provided, single submitter clinical testing c.736-9C>T in intron 8 of MYH6: This variant is not expected to have clinical si gnificance because a C>T change at this position does not diverge from the splic e consensus sequence and is therefore unlikely to impact splicing.
Invitae RCV000456853 SCV000557896 likely benign not provided 2016-11-09 criteria provided, single submitter clinical testing

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