List of variants reported as pathogenic for Cardiomyopathy, familial hypertrophic 27 by OMIM

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Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_020778.5(ALPK3):c.3175C>T (p.Arg1059Ter)	rs749465164	0.00004
NM_020778.5(ALPK3):c.4130-1G>A	rs762110595	0.00002
ALPK3, 2-BP DEL, 1531AA
NM_020778.5(ALPK3):c.-66del	rs974266035
NM_020778.5(ALPK3):c.2833C>T (p.Arg945Trp)
NM_020778.5(ALPK3):c.3186G>A (p.Trp1062Ter)	rs1555435531
NM_020778.5(ALPK3):c.4549G>C (p.Ala1517Pro)
NM_020778.5(ALPK3):c.4688G>A (p.Trp1563Ter)	rs1555436118

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