List of variants reported as pathogenic for Hypertrophic cardiomyopathy 11 by OMIM

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_005159.5(ACTC1):c.268C>T (p.His90Tyr)	rs121912676	0.00001
NM_005159.5(ACTC1):c.301G>A (p.Glu101Lys)	rs193922680	0.00001
NM_005159.5(ACTC1):c.496C>G (p.Pro166Ala)	rs267606628
NM_005159.5(ACTC1):c.889G>T (p.Ala297Ser)	rs121912675
NM_005159.5(ACTC1):c.997G>C (p.Ala333Pro)	rs267606629

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