ClinVar Miner

List of variants reported as likely pathogenic for Hypertrophic cardiomyopathy 26 by Institute of Human Genetics, Heidelberg University

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001458.5(FLNC):c.6893C>A (p.Pro2298His)	rs1382734231	0.00001
NM_001458.5(FLNC):c.7235_7236del (p.Thr2412fs)	rs776889134

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