ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.35186AAG[1] (p.Glu11730del)

dbSNP: rs1348719464
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV001699631 SCV004152471 uncertain significance not provided 2023-07-01 criteria provided, single submitter clinical testing TTN: PM4
Clinical Genetics, Academic Medical Center RCV001699631 SCV001922177 uncertain significance not provided no assertion criteria provided clinical testing
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen RCV001699631 SCV001963007 uncertain significance not provided no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001699631 SCV001980169 uncertain significance not provided no assertion criteria provided clinical testing

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