ClinVar Miner

List of variants in gene TXNRD2 reported as benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 70
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HGVS dbSNP gnomAD frequency
NM_006440.5(TXNRD2):c.1109T>C (p.Ile370Thr) rs1139793 0.77627
NM_006440.5(TXNRD2):c.173-70T>C rs5748471 0.65367
NM_006440.5(TXNRD2):c.662+63T>C rs885987 0.65001
NM_006440.5(TXNRD2):c.375-62C>T rs756661 0.64823
NM_006440.5(TXNRD2):c.374+77G>C rs3747067 0.60365
NM_006440.5(TXNRD2):c.950-220A>G rs5992492 0.53820
NM_006440.5(TXNRD2):c.177C>T (p.Ala59=) rs5748470 0.50192
NM_006440.5(TXNRD2):c.529-97G>A rs2073771 0.38130
NM_006440.5(TXNRD2):c.374+287G>A rs5993865 0.37953
NM_006440.5(TXNRD2):c.196G>T (p.Ala66Ser) rs5748469 0.35646
NM_006440.5(TXNRD2):c.1276-234C>G rs5993849 0.28479
NM_006440.5(TXNRD2):c.1206G>A (p.Pro402=) rs1139795 0.27722
NM_006440.5(TXNRD2):c.1275+163G>C rs11913319 0.26472
NM_006440.5(TXNRD2):c.949+300C>T rs5993856 0.25693
NM_006440.5(TXNRD2):c.774+14C>A rs12169091 0.25670
NM_006440.5(TXNRD2):c.1086+17G>A rs2239893 0.25106
NM_006440.5(TXNRD2):c.950-113G>C rs13057374 0.24893
NM_006440.5(TXNRD2):c.246C>T (p.Leu82=) rs11541479 0.20721
NM_006440.5(TXNRD2):c.173-224A>G rs17745433 0.15975
NM_006440.5(TXNRD2):c.1183-120G>T rs13054713 0.15188
NM_006440.5(TXNRD2):c.662+14G>A rs9606176 0.13466
NM_006440.5(TXNRD2):c.374+127C>T rs34751052 0.13405
NM_006440.5(TXNRD2):c.*254A>G rs1044732 0.12023
NM_006440.5(TXNRD2):c.*65+228C>T rs7287073 0.11200
NM_006440.5(TXNRD2):c.591+211A>G rs4597638 0.10467
NM_006440.5(TXNRD2):c.949+42C>T rs5992494 0.10038
NM_006440.5(TXNRD2):c.103+197G>A rs13306278 0.09627
NM_006440.5(TXNRD2):c.1347+20A>G rs113605285 0.08271
NM_006440.5(TXNRD2):c.775-85T>C rs78239309 0.05915
NM_006440.5(TXNRD2):c.591+66G>A rs16982755 0.05072
NM_006440.5(TXNRD2):c.375-128C>A rs34776119 0.04465
NM_006440.5(TXNRD2):c.682+129C>T rs76692419 0.04209
NM_006440.5(TXNRD2):c.449+111G>A rs77573782 0.04186
NM_006440.5(TXNRD2):c.1446-203G>A rs73381892 0.03871
NM_006440.5(TXNRD2):c.450-292C>T rs115268335 0.03523
NM_006440.5(TXNRD2):c.662+13C>T rs45550336 0.03292
NM_006440.5(TXNRD2):c.662+82G>T rs55715863 0.03288
NM_006440.5(TXNRD2):c.592-91C>G rs16982754 0.03284
NM_006440.5(TXNRD2):c.1275+198T>C rs76576226 0.02860
NM_006440.5(TXNRD2):c.950-214G>A rs114054391 0.02434
NM_006440.5(TXNRD2):c.526G>C (p.Glu176Gln) rs61736929 0.02373
NM_006440.5(TXNRD2):c.529-118C>G rs114905700 0.02202
NM_006440.5(TXNRD2):c.529-98C>T rs116165976 0.02181
NM_006440.5(TXNRD2):c.375-204T>C rs10427871 0.02130
NM_006440.5(TXNRD2):c.374+13C>T rs9606178 0.02112
NM_006440.5(TXNRD2):c.592-27T>C rs77585626 0.02084
NM_006440.5(TXNRD2):c.1445+254G>A rs16984300 0.01804
NM_006440.5(TXNRD2):c.1099C>T (p.Leu367=) rs35544159 0.01575
NM_006440.5(TXNRD2):c.1445+18C>T rs41431147 0.01166
NM_006440.5(TXNRD2):c.1233C>T (p.Ser411=) rs35099271 0.00966
NM_006440.5(TXNRD2):c.591+18del rs200848663 0.00807
NM_006440.5(TXNRD2):c.529-6C>T rs116054286 0.00525
NM_006440.5(TXNRD2):c.1087-11C>T rs577814757 0.00505
NM_006440.5(TXNRD2):c.110A>T (p.Gln37Leu) rs148092370 0.00150
NM_006440.5(TXNRD2):c.*239del rs59339361
NM_006440.5(TXNRD2):c.1087-16del rs34827823
NM_006440.5(TXNRD2):c.1150G>A (p.Gly384Ser) rs192869629
NM_006440.5(TXNRD2):c.173-131_173-130insGGCCAGAGCGCAGAGGCAGATCAGGGGTCCCTAGCATTGCGCAGCTCAGCG rs71324515
NM_006440.5(TXNRD2):c.230-168_230-167del rs146802029
NM_006440.5(TXNRD2):c.374+16C>A rs141500917
NM_006440.5(TXNRD2):c.592-246G>C rs79099740
NM_006440.5(TXNRD2):c.662+240del rs149796774
NM_006440.5(TXNRD2):c.662+281_662+282dup rs55813218
NM_006440.5(TXNRD2):c.662+281dup rs55813218
NM_006440.5(TXNRD2):c.663-206C>T rs8142006
NM_006440.5(TXNRD2):c.763G>C (p.Gly255Arg) rs76079250
NM_006440.5(TXNRD2):c.895A>C (p.Ser299Arg) rs5992495
NM_006440.5(TXNRD2):c.903C>A (p.Thr301=) rs35695986
NM_006440.5(TXNRD2):c.949+421dup rs35599379
NM_006440.5(TXNRD2):c.949+437del rs35599379

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