ClinVar Miner

List of variants in gene TNNI3 reported as likely benign for Familial Hypertrophic Cardiomyopathy with Wolff-Parkinson-White Syndrome

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Total variants: 9
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HGVS dbSNP gnomAD frequency
NM_000363.5(TNNI3):c.198G>A (p.Glu66=) rs3729710 0.03372
NM_000363.5(TNNI3):c.244C>T (p.Pro82Ser) rs77615401 0.00699
NM_000363.4(TNNI3):c.-148A>G rs73935313 0.00695
NM_000363.5(TNNI3):c.-47C>T rs202159627 0.00625
NM_000363.5(TNNI3):c.273G>A (p.Ala91=) rs75491697 0.00198
NM_000363.5(TNNI3):c.373-15C>G rs192630178 0.00141
NM_000363.5(TNNI3):c.235C>T (p.Arg79Cys) rs3729712 0.00048
NM_000363.5(TNNI3):c.*35C>T rs375447438 0.00004
NM_000363.5(TNNI3):c.-98C>A rs12973773

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