ClinVar Miner

Submissions for variant NM_001458.5(FLNC):c.7581del (p.Ile2527fs)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Human Genetics, University of Leuven RCV003164444 SCV002581942 likely pathogenic Primary familial dilated cardiomyopathy 2021-12-24 criteria provided, single submitter clinical testing
Baylor Genetics RCV003333215 SCV004041264 likely pathogenic Myofibrillar myopathy 5 2023-07-07 criteria provided, single submitter clinical testing
Baylor Genetics RCV003333217 SCV004041459 likely pathogenic Hypertrophic cardiomyopathy 26 2023-07-07 criteria provided, single submitter clinical testing
Baylor Genetics RCV003333216 SCV004041486 likely pathogenic Distal myopathy with posterior leg and anterior hand involvement 2023-07-07 criteria provided, single submitter clinical testing

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