List of variants reported as likely pathogenic for Hypertrophic cardiomyopathy by Genetics and Genomics Program, Sidra Medicine

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_004453.4(ETFDH):c.572G>A (p.Gly191Asp)	rs147219158	0.00034
NM_000257.4(MYH7):c.1988G>A (p.Arg663His)	rs371898076	0.00005
NM_003365.3(UQCRC1):c.826C>T (p.Arg276Cys)	rs201911056	0.00002
NM_001276345.2(TNNT2):c.886C>T (p.Arg296Cys)	rs367785431	0.00001
NM_000256.3(MYBPC3):c.3009_3010del (p.Gln1004fs)	rs2095879705
NM_000256.3(MYBPC3):c.51dup (p.Ser18fs)	rs1595850762

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