List of variants reported as pathogenic for Primary familial hypertrophic cardiomyopathy by Clinical Center for Gene Diagnosis and Therapy, Department of Cardiovascular Surgery, The Second Xiangya Hospital of Central South University

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000256.3(MYBPC3):c.2459G>A (p.Arg820Gln)	rs2856655	0.00002
NM_000257.4(MYH7):c.1357C>T (p.Arg453Cys)	rs121913625	0.00001
NM_000257.4(MYH7):c.1816G>A (p.Val606Met)	rs121913627	0.00001
NM_000257.4(MYH7):c.5134C>T (p.Arg1712Trp)	rs121913650

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