ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.38465-14T>C

gnomAD frequency: 0.00002  dbSNP: rs887421079
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV001699917 SCV001926409 likely benign not provided no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001699917 SCV001970080 likely benign not provided no assertion criteria provided clinical testing

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