ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.16621+16T>G

dbSNP: rs2154310257
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen RCV001529685 SCV001743552 likely benign not provided no assertion criteria provided clinical testing
Clinical Genetics, Academic Medical Center RCV001700781 SCV001924883 benign not specified no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001529685 SCV001966225 likely benign not provided no assertion criteria provided clinical testing

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