ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.82979T>C (p.Leu27660Pro)

gnomAD frequency: 0.00001  dbSNP: rs1222575627
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Clinical Genetics, Academic Medical Center RCV001699856 SCV001922112 uncertain significance not provided no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001699856 SCV001972258 uncertain significance not provided no assertion criteria provided clinical testing

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