ClinVar Miner

Submissions for variant NM_001458.5(FLNC):c.6429G>T (p.Gln2143His)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics, University of Wuerzburg RCV003444007 SCV004171041 uncertain significance Hypertrophic cardiomyopathy 26 no assertion criteria provided clinical testing

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