ClinVar Miner

List of variants in gene TNNI3 reported as uncertain significance for Primary familial hypertrophic cardiomyopathy

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Total variants: 4
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HGVS dbSNP
NM_000363.5(TNNI3):c.307C>T (p.Arg103Cys) rs397516344
NM_000363.5(TNNI3):c.484C>T (p.Arg162Trp) rs368861241
NM_000363.5(TNNI3):c.549+68_549+69insGGCCTA rs139158921
NM_000363.5(TNNI3):c.566G>A (p.Gly189Glu) rs587782980

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