ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.85809del (p.Lys28603fs)

dbSNP: rs796983799
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
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen RCV001528480 SCV001740300 likely pathogenic not provided no assertion criteria provided clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV001528480 SCV001931646 pathogenic not provided no assertion criteria provided clinical testing

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