ClinVar Miner

Submissions for variant NM_001458.4(FLNC):c.2390-9T>C (rs368068407)

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Total submissions: 6
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001083797 SCV000650945 benign Myofibrillar myopathy, filamin C-related; Myopathy, distal, 4; Cardiomyopathy, familial hypertrophic, 26; Dilated Cardiomyopathy, Dominant 2020-12-08 criteria provided, single submitter clinical testing
GeneDx RCV000528872 SCV000732087 benign not provided 2021-01-15 criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV000528872 SCV001143943 benign not provided 2019-04-01 criteria provided, single submitter clinical testing
Clinical Genetics,Academic Medical Center RCV000606796 SCV001919971 benign not specified no assertion criteria provided clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV000606796 SCV001928084 benign not specified no assertion criteria provided clinical testing
Human Genetics - Radboudumc,Radboudumc RCV000528872 SCV001951785 likely benign not provided no assertion criteria provided clinical testing

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