ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.72104T>G (p.Phe24035Cys)

dbSNP: rs759861907
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Revvity Omics, Revvity RCV001699611 SCV004237036 uncertain significance not provided 2023-06-14 criteria provided, single submitter clinical testing
Clinical Genetics, Academic Medical Center RCV001699611 SCV001922689 uncertain significance not provided no assertion criteria provided clinical testing
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen RCV001699611 SCV001963106 uncertain significance not provided no assertion criteria provided clinical testing

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