ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.50653A>G (p.Ile16885Val)

dbSNP: rs1405647586
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Total submissions: 2
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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 RCV001730316 SCV001978644 uncertain significance not provided no assertion criteria provided clinical testing
Clinical Genetics, Academic Medical Center RCV001730316 SCV001978822 uncertain significance not provided no assertion criteria provided clinical testing

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