ClinVar Miner

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

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Gene type:
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Total variants: 32
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HGVS dbSNP
NM_006440.5(TXNRD2):c.103+81dup rs45511293
NM_006440.5(TXNRD2):c.1158C>T (p.Ser386=) rs558954630
NM_006440.5(TXNRD2):c.1275+163G>C rs11913319
NM_006440.5(TXNRD2):c.1275+198T>C rs76576226
NM_006440.5(TXNRD2):c.1276-234C>G rs5993849
NM_006440.5(TXNRD2):c.1445+254G>A rs16984300
NM_006440.5(TXNRD2):c.1446-203G>A rs73381892
NM_006440.5(TXNRD2):c.173-224A>G rs17745433
NM_006440.5(TXNRD2):c.173-70T>C rs5748471
NM_006440.5(TXNRD2):c.230-168_230-167del rs146802029
NM_006440.5(TXNRD2):c.374+127C>T rs34751052
NM_006440.5(TXNRD2):c.374+287G>A rs5993865
NM_006440.5(TXNRD2):c.374+77G>C rs3747067
NM_006440.5(TXNRD2):c.375-128C>A rs34776119
NM_006440.5(TXNRD2):c.375-62C>T rs756661
NM_006440.5(TXNRD2):c.449+111G>A rs77573782
NM_006440.5(TXNRD2):c.450-292C>T rs115268335
NM_006440.5(TXNRD2):c.529-118C>G rs114905700
NM_006440.5(TXNRD2):c.529-97G>A rs2073771
NM_006440.5(TXNRD2):c.591+211A>G rs4597638
NM_006440.5(TXNRD2):c.591+66G>A rs16982755
NM_006440.5(TXNRD2):c.662+240del rs149796774
NM_006440.5(TXNRD2):c.662+63T>C rs885987
NM_006440.5(TXNRD2):c.663-206C>T rs8142006
NM_006440.5(TXNRD2):c.683-6C>T rs757160421
NM_006440.5(TXNRD2):c.68C>A (p.Ala23Glu) rs532340383
NM_006440.5(TXNRD2):c.775-85T>C rs78239309
NM_006440.5(TXNRD2):c.949+300C>T rs5993856
NM_006440.5(TXNRD2):c.949+42C>T rs5992494
NM_006440.5(TXNRD2):c.950-113G>C rs13057374
NM_006440.5(TXNRD2):c.950-214G>A rs114054391
NM_006440.5(TXNRD2):c.950-220A>G rs5992492

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