ClinVar Miner

List of variants in gene TNNT2 reported as pathogenic by Stanford Center for Inherited Cardiovascular Disease, Stanford University

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Total variants: 7
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HGVS dbSNP gnomAD frequency
NM_001276345.2(TNNT2):c.304C>T (p.Arg102Trp) rs397516456 0.00001
NM_001276345.2(TNNT2):c.305G>A (p.Arg102Gln) rs121964856 0.00001
NM_001276345.2(TNNT2):c.266T>A (p.Ile89Asn) rs121964855
NM_001276345.2(TNNT2):c.305G>T (p.Arg102Leu) rs121964856
NM_001276345.2(TNNT2):c.358T>A (p.Phe120Ile) rs121964858
NM_001276345.2(TNNT2):c.508GAG[3] (p.Glu173del) rs397516470
NM_001276345.2(TNNT2):c.650AGA[3] (p.Lys220del) rs45578238

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