ClinVar Miner

List of variants in gene TXNRD2 reported as likely benign for not provided

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Gene type:
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Total variants: 30
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HGVS dbSNP
NM_006440.5(TXNRD2):c.1029G>A (p.Val343=) rs758006460
NM_006440.5(TXNRD2):c.103+278C>T rs45559342
NM_006440.5(TXNRD2):c.104-102C>T rs79960807
NM_006440.5(TXNRD2):c.1087-8T>C rs1000041198
NM_006440.5(TXNRD2):c.1104A>G (p.Thr368=) rs1601384637
NM_006440.5(TXNRD2):c.1122C>T (p.Ala374=) rs780948248
NM_006440.5(TXNRD2):c.1176C>T (p.Tyr392=) rs544242322
NM_006440.5(TXNRD2):c.1182+49C>T rs73381902
NM_006440.5(TXNRD2):c.1398T>C (p.Leu466=) rs781691483
NM_006440.5(TXNRD2):c.1401C>T (p.Gly467=) rs886038873
NM_006440.5(TXNRD2):c.1446-70C>T rs116583868
NM_006440.5(TXNRD2):c.1464G>A (p.Ala488=) rs372816982
NM_006440.5(TXNRD2):c.1479C>T (p.Thr493=) rs767844402
NM_006440.5(TXNRD2):c.172+182C>T rs114490696
NM_006440.5(TXNRD2):c.264C>T (p.Asn88=) rs575321083
NM_006440.5(TXNRD2):c.374+87C>A rs138368791
NM_006440.5(TXNRD2):c.450-75G>C rs79661740
NM_006440.5(TXNRD2):c.591+243C>G rs145232439
NM_006440.5(TXNRD2):c.63C>T (p.Ala21=) rs562298402
NM_006440.5(TXNRD2):c.682+15C>T rs201450101
NM_006440.5(TXNRD2):c.714C>T (p.Thr238=) rs202225486
NM_006440.5(TXNRD2):c.756C>T (p.Pro252=) rs1371426999
NM_006440.5(TXNRD2):c.774+255C>A rs144567421
NM_006440.5(TXNRD2):c.849G>T (p.Arg283=) rs559964753
NM_006440.5(TXNRD2):c.903C>T (p.Thr301=) rs35695986
NM_006440.5(TXNRD2):c.912G>A (p.Glu304=) rs751531927
NM_006440.5(TXNRD2):c.939G>A (p.Leu313=) rs1060504228
NM_006440.5(TXNRD2):c.949+10C>T rs563775080
NM_006440.5(TXNRD2):c.950-80C>G rs145029690
NM_006440.5(TXNRD2):c.987G>A (p.Lys329=) rs1454322676

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