ClinVar Miner

List of variants in gene TXNRD2 reported as uncertain significance for Cardiovascular phenotype

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Total variants: 13
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HGVS dbSNP
NM_006440.5(TXNRD2):c.113G>A (p.Arg38Gln) rs777384922
NM_006440.5(TXNRD2):c.1289A>C (p.His430Pro) rs376463546
NM_006440.5(TXNRD2):c.1406A>G (p.Asn469Ser) rs757704344
NM_006440.5(TXNRD2):c.1511T>C (p.Val504Ala) rs769258408
NM_006440.5(TXNRD2):c.1514T>A (p.Val505Asp) rs759613137
NM_006440.5(TXNRD2):c.350T>C (p.Val117Ala) rs770727890
NM_006440.5(TXNRD2):c.431G>A (p.Arg144His) rs748674090
NM_006440.5(TXNRD2):c.46C>T (p.Arg16Trp) rs777650793
NM_006440.5(TXNRD2):c.529-5C>T rs766288973
NM_006440.5(TXNRD2):c.581A>G (p.Tyr194Cys) rs1219814151
NM_006440.5(TXNRD2):c.656G>C (p.Gly219Ala) rs199510610
NM_006440.5(TXNRD2):c.763G>A (p.Gly255Ser) rs76079250
NM_006440.5(TXNRD2):c.869G>T (p.Gly290Val) rs543290126

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