ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.74080G>T (p.Glu24694Ter)

dbSNP: rs2468519578
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics, University of Wuerzburg RCV002511508 SCV002820892 likely pathogenic Cardiomyopathy no assertion criteria provided clinical testing

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