ClinVar Miner

Submissions for variant NM_001458.5(FLNC):c.6005-7T>C

dbSNP: rs1585167904
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001498484 SCV001703234 likely benign Myofibrillar myopathy 5; Distal myopathy with posterior leg and anterior hand involvement; Hypertrophic cardiomyopathy 26; Dilated Cardiomyopathy, Dominant 2023-11-28 criteria provided, single submitter clinical testing

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