ClinVar Miner

List of variants in gene TXNRD2 reported as uncertain significance for Primary familial hypertrophic cardiomyopathy

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Total variants: 5
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NM_006440.5(TXNRD2):c.1321C>T (p.Arg441Ter) rs200162480
NM_006440.5(TXNRD2):c.174C>T (p.Ala58=) rs767236339
NM_006440.5(TXNRD2):c.236G>T (p.Arg79Leu) rs373979810
NM_006440.5(TXNRD2):c.337T>C (p.Tyr113His) rs869025560
NM_006440.5(TXNRD2):c.572G>A (p.Arg191Gln) rs730880248

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