ClinVar Miner

Submissions for variant NM_133379.5(TTN):c.13290T>C (p.Ser4430=)

gnomAD frequency: 0.00002  dbSNP: rs571273316
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Clinical Genetics, Academic Medical Center RCV001699979 SCV001917197 benign not specified no assertion criteria provided clinical testing
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen RCV001726642 SCV001962988 likely benign not provided no assertion criteria provided clinical testing

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