ClinVar Miner

Submissions for variant NM_015978.3(TNNI3K):c.827+11T>C

gnomAD frequency: 0.00080  dbSNP: rs148757567
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002206186 SCV002491876 benign not provided 2025-01-28 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV005232911 SCV004562118 benign Atrial conduction disease 2024-03-11 criteria provided, single submitter clinical testing

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