ClinVar Miner

Submissions for variant NM_001458.5(FLNC):c.4346C>G (p.Ser1449Ter)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Human Genetics, University of Leuven RCV003164449 SCV002581948 likely pathogenic Primary familial dilated cardiomyopathy 2021-12-24 criteria provided, single submitter clinical testing

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