ClinVar Miner

Submissions for variant NM_000363.5(TNNI3):c.373-15del

dbSNP: rs2515498727
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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 RCV002954064 SCV003279820 benign Hypertrophic cardiomyopathy 2022-12-06 criteria provided, single submitter clinical testing

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