ClinVar Miner

Submissions for variant NM_015978.3(TNNI3K):c.1878+10T>C

gnomAD frequency: 0.00038  dbSNP: rs199892485
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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 RCV000887911 SCV001031503 benign not provided 2025-01-27 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV005231940 SCV005878317 benign Atrial conduction disease 2024-07-25 criteria provided, single submitter clinical testing

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