ClinVar Miner

Submissions for variant NM_133379.5(TTN):c.15318T>C (p.Tyr5106=)

dbSNP: rs569499266
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000593200 SCV000702057 likely benign not specified 2016-10-18 criteria provided, single submitter clinical testing
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen RCV001528394 SCV001740083 likely benign not provided no assertion criteria provided clinical testing
Laboratory of Diagnostic Genome Analysis, Leiden University Medical Center (LUMC) RCV001528394 SCV001798043 likely benign not provided no assertion criteria provided clinical testing

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