List of variants reported as likely benign for Hypertrophic cardiomyopathy 19 by Genome Diagnostics Laboratory, University Medical Center Utrecht

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_145046.5(CALR3):c.398-6T>C	rs376479901	0.00114
NM_145046.5(CALR3):c.125A>G (p.Asn42Ser)	rs149634686	0.00113
NM_145046.5(CALR3):c.245A>G (p.Lys82Arg)	rs142951029	0.00083
NM_145046.5(CALR3):c.60C>G (p.Thr20=)	rs370721650	0.00029

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