ClinVar Miner

Submissions for variant NM_001458.4(FLNC):c.4296G>A (p.Pro1432=) (rs370827536)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Praxis fuer Humangenetik Tuebingen RCV000416169 SCV000493469 uncertain significance not provided 2016-07-31 criteria provided, single submitter clinical testing
Invitae RCV000526964 SCV000651025 likely benign Myofibrillar myopathy, filamin C-related; Myopathy, distal, 4; Cardiomyopathy, familial hypertrophic, 26; Dilated Cardiomyopathy, Dominant 2017-12-08 criteria provided, single submitter clinical testing

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