ClinVar Miner

Submissions for variant NM_133379.5(TTN):c.10842A>G (p.Glu3614=)

gnomAD frequency: 0.00001  dbSNP: rs796091067
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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 RCV001528782 SCV001741124 likely benign not provided no assertion criteria provided clinical testing
Laboratory of Diagnostic Genome Analysis, Leiden University Medical Center (LUMC) RCV001528782 SCV001799338 likely benign not provided no assertion criteria provided clinical testing
Clinical Genetics, Academic Medical Center RCV001699808 SCV001925704 benign not specified no assertion criteria provided clinical testing

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