ClinVar Miner

Submissions for variant NM_001110556.2(FLNA):c.4776del (p.Lys1593fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease, Montreal Heart Institute RCV005403882 SCV006065025 likely pathogenic Cardiovascular phenotype 2021-01-04 criteria provided, single submitter clinical testing

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