List of variants reported as pathogenic for cardiomyopathy, familial hypertrophic, 23, with or without ventricular noncompaction by OMIM

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001103.4(ACTN2):c.1484C>T (p.Thr495Met)	rs200248944	0.00027
NM_001103.4(ACTN2):c.1883A>G (p.Glu628Gly)	rs786204951
NM_001103.4(ACTN2):c.2276G>C (p.Arg759Thr)	rs786204950
NM_001103.4(ACTN2):c.332G>T (p.Gly111Val)	rs786204949
NM_001103.4(ACTN2):c.355G>A (p.Ala119Thr)	rs727502886

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