ClinVar Miner

Submissions for variant NM_002471.4(MYH6):c.3105+9T>C

dbSNP: rs1555333942
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000552239 SCV000648242 likely benign Hypertrophic cardiomyopathy 14 2017-04-26 criteria provided, single submitter clinical testing
Blueprint Genetics RCV000788242 SCV000927293 uncertain significance not provided 2017-06-14 criteria provided, single submitter clinical testing

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