ClinVar Miner

Submissions for variant NM_000363.5(TNNI3):c.108+21G>A

gnomAD frequency: 0.04872  dbSNP: rs3729837
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000250795 SCV000303829 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001658163 SCV001873496 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ RCV000250795 SCV001958060 benign not specified no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV000250795 SCV001971297 benign not specified no assertion criteria provided clinical testing

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