ClinVar Miner

List of variants in gene TXNRD2 reported as likely benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 82
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_006440.5(TXNRD2):c.104-102C>T rs79960807 0.01811
NM_006440.5(TXNRD2):c.1275+233T>C rs11913382 0.01455
NM_006440.5(TXNRD2):c.375-152G>A rs113107030 0.01356
NM_006440.5(TXNRD2):c.1182+49C>T rs73381902 0.01336
NM_006440.5(TXNRD2):c.172+182C>T rs114490696 0.01325
NM_006440.5(TXNRD2):c.950-80C>G rs145029690 0.01268
NM_006440.5(TXNRD2):c.103+278C>T rs45559342 0.01062
NM_006440.5(TXNRD2):c.1446-70C>T rs116583868 0.00787
NM_006440.5(TXNRD2):c.774+255C>A rs144567421 0.00769
NM_006440.5(TXNRD2):c.1183-82C>T rs146159731 0.00537
NM_006440.5(TXNRD2):c.375-19T>G rs147120537 0.00527
NM_006440.5(TXNRD2):c.663-134G>A rs7292942 0.00508
NM_006440.5(TXNRD2):c.591+196C>T rs78146516 0.00474
NM_006440.5(TXNRD2):c.450-232T>C rs188325304 0.00422
NM_006440.5(TXNRD2):c.374+87C>A rs138368791 0.00404
NM_006440.5(TXNRD2):c.1087-243G>A rs113856303 0.00327
NM_006440.5(TXNRD2):c.816C>T (p.Gly272=) rs144584524 0.00266
NM_006440.5(TXNRD2):c.505G>A (p.Gly169Ser) rs138462062 0.00128
NM_006440.5(TXNRD2):c.933C>T (p.Thr311=) rs187065627 0.00108
NM_006440.5(TXNRD2):c.1016A>T (p.Gln339Leu) rs200606822 0.00106
NM_006440.5(TXNRD2):c.1195G>A (p.Val399Ile) rs201222740 0.00104
NM_006440.5(TXNRD2):c.1523G>A (p.Arg508His) rs201391000 0.00102
NM_006440.5(TXNRD2):c.762C>T (p.Arg254=) rs180876642 0.00101
NM_006440.5(TXNRD2):c.374+17G>A rs200108545 0.00080
NM_006440.5(TXNRD2):c.303A>G (p.Ala101=) rs200076623 0.00069
NM_006440.5(TXNRD2):c.858G>C (p.Arg286Ser) rs201503021 0.00064
NM_006440.5(TXNRD2):c.1461T>C (p.Tyr487=) rs376363162 0.00061
NM_006440.5(TXNRD2):c.775-19G>A rs189646218 0.00048
NM_006440.5(TXNRD2):c.1509G>A (p.Glu503=) rs200619889 0.00045
NM_006440.5(TXNRD2):c.592-17C>A rs375350567 0.00044
NM_006440.5(TXNRD2):c.656G>C (p.Gly219Ala) rs199510610 0.00042
NM_006440.5(TXNRD2):c.375-8C>T rs180876844 0.00041
NM_006440.5(TXNRD2):c.462C>T (p.Tyr154=) rs182857388 0.00038
NM_006440.5(TXNRD2):c.662+11C>G rs373734411 0.00038
NM_006440.5(TXNRD2):c.1308C>T (p.Phe436=) rs190301927 0.00031
NM_006440.5(TXNRD2):c.229+15A>G rs370756162 0.00029
NM_006440.5(TXNRD2):c.957C>G (p.Val319=) rs371700934 0.00024
NM_006440.5(TXNRD2):c.1275+18C>T rs374333900 0.00023
NM_006440.5(TXNRD2):c.1077C>T (p.Asp359=) rs147383232 0.00021
NM_006440.5(TXNRD2):c.1086+12G>A rs143966577 0.00021
NM_006440.5(TXNRD2):c.683-6C>T rs757160421 0.00021
NM_006440.5(TXNRD2):c.1137G>C (p.Val379=) rs184640901 0.00020
NM_006440.5(TXNRD2):c.173-19del rs770032943 0.00020
NM_006440.5(TXNRD2):c.229+24G>A rs79850332 0.00020
NM_006440.5(TXNRD2):c.1155G>C (p.Gly385=) rs370957634 0.00019
NM_006440.5(TXNRD2):c.585C>G (p.Pro195=) rs201760306 0.00019
NM_006440.5(TXNRD2):c.682+15C>T rs201450101 0.00017
NM_006440.5(TXNRD2):c.834C>G (p.Gly278=) rs371075332 0.00016
NM_006440.5(TXNRD2):c.1182+20G>A rs369759249 0.00014
NM_006440.5(TXNRD2):c.1276-15G>A rs374202570 0.00014
NM_006440.5(TXNRD2):c.949+238C>T rs529169039 0.00011
NM_006440.5(TXNRD2):c.1224G>C (p.Val408=) rs375650172 0.00009
NM_006440.5(TXNRD2):c.949+11G>A rs772807846 0.00007
NM_006440.5(TXNRD2):c.1176C>T (p.Tyr392=) rs544242322 0.00006
NM_006440.5(TXNRD2):c.1445+13G>T rs938029725 0.00006
NM_006440.5(TXNRD2):c.174C>T (p.Ala58=) rs767236339 0.00006
NM_006440.5(TXNRD2):c.528+19C>T rs746285839 0.00006
NM_006440.5(TXNRD2):c.1182+19C>T rs377040175 0.00004
NM_006440.5(TXNRD2):c.1368C>T (p.Pro456=) rs1388056453 0.00004
NM_006440.5(TXNRD2):c.1497A>G (p.Thr499=) rs969582646 0.00004
NM_006440.5(TXNRD2):c.449+4C>T rs755751835 0.00004
NM_006440.5(TXNRD2):c.1464G>A (p.Ala488=) rs372816982 0.00003
NM_006440.5(TXNRD2):c.449+17C>T rs370505160 0.00003
NM_006440.5(TXNRD2):c.489C>T (p.Asp163=) rs751116028 0.00003
NM_006440.5(TXNRD2):c.1086+11C>T rs369332144 0.00002
NM_006440.5(TXNRD2):c.1122C>T (p.Ala374=) rs780948248 0.00002
NM_006440.5(TXNRD2):c.172+20C>A rs760016716 0.00001
NM_006440.5(TXNRD2):c.366G>A (p.Pro122=) rs3747068 0.00001
NM_006440.5(TXNRD2):c.588G>A (p.Thr196=) rs377699868 0.00001
NM_006440.5(TXNRD2):c.*239dup rs59339361
NM_006440.5(TXNRD2):c.1107C>A (p.Pro369=) rs371533709
NM_006440.5(TXNRD2):c.1407C>A (p.Asn469Lys) rs200063300
NM_006440.5(TXNRD2):c.173-15T>C rs1555913241
NM_006440.5(TXNRD2):c.450-15_450-14del rs767787404
NM_006440.5(TXNRD2):c.450-274C>A rs137960501
NM_006440.5(TXNRD2):c.450-75G>C rs79661740
NM_006440.5(TXNRD2):c.529-8C>T rs754998172
NM_006440.5(TXNRD2):c.591+243C>G rs145232439
NM_006440.5(TXNRD2):c.592-20G>C rs1555911999
NM_006440.5(TXNRD2):c.592-5G>C rs1555911995
NM_006440.5(TXNRD2):c.682+16G>A rs377147143
NM_006440.5(TXNRD2):c.903C>T (p.Thr301=) rs35695986

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.