List of variants in gene TNNT2 reported as likely pathogenic for Hypertrophic cardiomyopathy

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_001276345.2(TNNT2):c.862C>T (p.Arg288Cys)	rs121964857	0.00044
NM_001276345.2(TNNT2):c.287A>C (p.Asp96Ala)	rs397516455	0.00001
NM_001276345.2(TNNT2):c.360T>G (p.Phe120Leu)	rs727504331	0.00001
NM_001276345.2(TNNT2):c.823C>T (p.Arg275Ter)	rs748970759	0.00001
NM_001276345.2(TNNT2):c.886C>T (p.Arg296Cys)	rs367785431	0.00001
NM_001276345.2(TNNT2):c.274G>A (p.Gly92Arg)	rs727504255
NM_001276345.2(TNNT2):c.307A>C (p.Lys103Gln)	rs730881122
NM_001276345.2(TNNT2):c.311G>T (p.Arg104Leu)	rs397516457
NM_001276345.2(TNNT2):c.316_318del (p.Glu106del)	rs727504277
NM_001276345.2(TNNT2):c.321G>T (p.Lys107Asn)	rs397516459
NM_001276345.2(TNNT2):c.566C>T (p.Ser189Phe)	rs727504246
NM_001276345.2(TNNT2):c.837C>A (p.Asn279Lys)	rs376923877
NM_001276345.2(TNNT2):c.851+1G>T	rs111377893
NM_001276345.2(TNNT2):c.891G>A (p.Trp297Ter)	rs730881116

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