ClinVar Miner

List of variants reported as likely pathogenic for Familial hypertrophic cardiomyopathy 2

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Total variants: 5
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HGVS dbSNP
NM_000364.4(TNNT2):c.305G>A (p.Arg102Gln) rs121964856
NM_000364.4(TNNT2):c.653T>C (p.Ile218Thr) rs863225120
NM_000364.4(TNNT2):c.833A>T (p.Asn278Ile) rs863225119
NM_000364.4(TNNT2):c.842+1G>C rs111377893
NM_000364.4(TNNT2):c.881G>A (p.Trp294Ter) rs727504247

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