ClinVar Miner

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

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Total variants: 3
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HGVS dbSNP
NM_006393.3(NEBL):c.267C>G (p.Tyr89Ter) rs147622517
NM_213569.2(NEBL):c.305C>T (p.Thr102Met) rs377492976
NM_213569.2(NEBL):c.358-27882G>T rs201103536

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