ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.23674A>G (p.Ile7892Val)

dbSNP: rs2078060561
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Revvity Omics, Revvity RCV001699624 SCV003826676 uncertain significance not provided 2022-11-10 criteria provided, single submitter clinical testing
Clinical Genetics, Academic Medical Center RCV001699624 SCV001920200 uncertain significance not provided no assertion criteria provided clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV001699624 SCV001931751 uncertain significance not provided no assertion criteria provided clinical testing

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