ClinVar Miner

List of variants in gene TNNT2 reported as uncertain significance for Primary familial hypertrophic cardiomyopathy

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Total variants: 5
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HGVS dbSNP
NM_000364.4(TNNT2):c.260C>T (p.Pro87Leu) rs144900708
NM_000364.4(TNNT2):c.601A>G (p.Thr201Ala) rs587782981
NM_000364.4(TNNT2):c.753G>T (p.Glu251Asp) rs45466197
NM_000364.4(TNNT2):c.869T>A (p.Val290Asp) rs730880233
NM_000364.4(TNNT2):c.874G>A (p.Gly292Arg) rs147940106

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