ClinVar Miner

Submissions for variant NM_015978.3(TNNI3K):c.1620A>G (p.Gln540=)

dbSNP: rs55654209
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000967917 SCV001115341 benign not provided 2025-01-31 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000967917 SCV005280842 benign not provided criteria provided, single submitter not provided
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV005232005 SCV005879270 benign Atrial conduction disease 2024-05-14 criteria provided, single submitter clinical testing
Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease, Montreal Heart Institute RCV005405454 SCV006069551 benign not specified 2025-04-09 criteria provided, single submitter clinical testing

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