List of variants reported as uncertain significance for Hypertrophic cardiomyopathy 4 by Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen

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Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_000256.3(MYBPC3):c.1321G>A (p.Glu441Lys)	rs193922377	0.00016
NM_000256.3(MYBPC3):c.529C>T (p.Arg177Cys)	rs193922385	0.00009
NM_000256.3(MYBPC3):c.2198G>A (p.Arg733His)	rs534345197	0.00003
NM_000256.3(MYBPC3):c.713G>A (p.Arg238His)	rs727504396	0.00002
NM_000256.3(MYBPC3):c.1766G>A (p.Arg589His)	rs397515923	0.00001
NM_000256.3(MYBPC3):c.2815C>T (p.Arg939Trp)	rs534366414	0.00001
NM_000256.3(MYBPC3):c.2927C>G (p.Pro976Arg)	rs954096716	0.00001
NM_000256.3(MYBPC3):c.3358C>T (p.Arg1120Cys)	rs368721523	0.00001
NM_000256.3(MYBPC3):c.3613C>T (p.Arg1205Trp)	rs727503171	0.00001
NM_000256.3(MYBPC3):c.194C>T (p.Thr65Met)	rs753300898

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