ClinVar Miner

Submissions for variant NM_000363.5(TNNI3):c.373-8G>C

dbSNP: rs369244036
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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 RCV000543001 SCV000623780 likely benign Hypertrophic cardiomyopathy 2019-02-06 criteria provided, single submitter clinical testing

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