List of variants reported as likely pathogenic for Hypertrophic cardiomyopathy 2 by Genome-Nilou Lab

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Total variants: 18

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HGVS	dbSNP	gnomAD frequency
NM_001276345.2(TNNT2):c.287A>C (p.Asp96Ala)	rs397516455	0.00001
NM_001276345.2(TNNT2):c.305G>A (p.Arg102Gln)	rs121964856	0.00001
NM_001276345.2(TNNT2):c.360T>G (p.Phe120Leu)	rs727504331	0.00001
NM_001276345.2(TNNT2):c.418C>T (p.Arg140Cys)	rs397516463	0.00001
NM_001276345.2(TNNT2):c.890G>A (p.Trp297Ter)	rs727504247	0.00001
NM_001276345.2(TNNT2):c.274G>A (p.Gly92Arg)	rs727504255
NM_001276345.2(TNNT2):c.310C>T (p.Arg104Cys)	rs727503513
NM_001276345.2(TNNT2):c.311G>T (p.Arg104Leu)	rs397516457
NM_001276345.2(TNNT2):c.321G>T (p.Lys107Asn)	rs397516459
NM_001276345.2(TNNT2):c.421C>T (p.Arg141Trp)	rs74315380
NM_001276345.2(TNNT2):c.422G>C (p.Arg141Pro)	rs397516464
NM_001276345.2(TNNT2):c.430C>G (p.Arg144Gly)	rs45525839
NM_001276345.2(TNNT2):c.548G>A (p.Arg183Gln)	rs397516471
NM_001276345.2(TNNT2):c.566C>T (p.Ser189Phe)	rs727504246
NM_001276345.2(TNNT2):c.650AGA[3] (p.Lys220del)	rs45578238
NM_001276345.2(TNNT2):c.851+1G>A	rs111377893
NM_001276345.2(TNNT2):c.851+1G>T	rs111377893
NM_001276345.2(TNNT2):c.891G>A (p.Trp297Ter)	rs730881116

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