List of variants reported as pathogenic for hypertrophic cardiomyopathy 6

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Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_016203.4(PRKAG2):c.905G>A (p.Arg302Gln)	rs121908987	0.00001
NM_016203.4(PRKAG2):c.1050_1051insTTA (p.Arg350_Glu351insLeu)	rs587776643
NM_016203.4(PRKAG2):c.1148A>G (p.His383Arg)	rs121908988
NM_016203.4(PRKAG2):c.1199C>A (p.Thr400Asn)	rs28938173
NM_016203.4(PRKAG2):c.1459T>C (p.Tyr487His)	rs267606976
NM_016203.4(PRKAG2):c.1463A>T (p.Asn488Ile)	rs121908989
NM_016203.4(PRKAG2):c.1516G>C (p.Glu506Gln)	rs267606978
NM_016203.4(PRKAG2):c.1589A>G (p.His530Arg)	rs267606977
NM_016203.4(PRKAG2):c.1642T>C (p.Ser548Pro)	rs267606979

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