ClinVar Miner

Submissions for variant NM_002471.4(MYH6):c.642+7T>C

dbSNP: rs1595064042
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001418466 SCV001620695 likely benign Hypertrophic cardiomyopathy 14 2018-08-29 criteria provided, single submitter clinical testing

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