ClinVar Miner

Submissions for variant NM_000363.5(TNNI3):c.12-1G>T

gnomAD frequency: 0.00001  dbSNP: rs397516340
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine RCV000036268 SCV000059920 likely pathogenic Hypertrophic cardiomyopathy 2008-03-01 no assertion criteria provided clinical testing

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