List of variants reported as likely pathogenic for Hypertrophic cardiomyopathy by ClinGen Cardiomyopathy Variant Curation Expert Panel

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Total variants: 18

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HGVS	dbSNP	gnomAD frequency
NM_000257.4(MYH7):c.2606G>A (p.Arg869His)	rs202141173	0.00009
NM_000257.4(MYH7):c.1370T>C (p.Ile457Thr)	rs397516103	0.00001
NM_000257.4(MYH7):c.3169G>A (p.Gly1057Ser)	rs397516179	0.00001
NM_000257.4(MYH7):c.3578G>A (p.Arg1193His)	rs397516187	0.00001
NM_000257.4(MYH7):c.4258C>T (p.Arg1420Trp)	rs145213771	0.00001
NM_000257.4(MYH7):c.428G>A (p.Arg143Gln)	rs397516209	0.00001
NM_000257.4(MYH7):c.1012G>A (p.Val338Met)	rs727503271
NM_000257.4(MYH7):c.1318G>A (p.Val440Met)	rs397516098
NM_000257.4(MYH7):c.2129C>A (p.Pro710His)	rs727504272
NM_000257.4(MYH7):c.2539_2541del (p.Lys847del)	rs397516155
NM_000257.4(MYH7):c.2593A>G (p.Lys865Glu)	rs730880749
NM_000257.4(MYH7):c.2602G>C (p.Ala868Pro)	rs727504356
NM_000257.4(MYH7):c.2608C>T (p.Arg870Cys)	rs138049878
NM_000257.4(MYH7):c.2785GAG[2] (p.Glu931del)	rs397516172
NM_000257.4(MYH7):c.2845G>A (p.Glu949Lys)	rs121913629
NM_000257.4(MYH7):c.3134G>T (p.Arg1045Leu)	rs397516178
NM_000257.4(MYH7):c.5134C>T (p.Arg1712Trp)	rs121913650
NM_000257.4(MYH7):c.715G>A (p.Asp239Asn)	rs397516264

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