ClinVar Miner

List of variants in gene TXNRD2 reported as uncertain significance by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 15
Download table as spreadsheet
NM_006440.5(TXNRD2):c.1016A>T (p.Gln339Leu) rs200606822
NM_006440.5(TXNRD2):c.1174T>C (p.Tyr392His) rs201971987
NM_006440.5(TXNRD2):c.1211A>G (p.Glu404Gly) rs1435686741
NM_006440.5(TXNRD2):c.1322G>A (p.Arg441Gln) rs759374389
NM_006440.5(TXNRD2):c.1407C>A (p.Asn469Lys) rs200063300
NM_006440.5(TXNRD2):c.1484G>A (p.Gly495Asp) rs773949487
NM_006440.5(TXNRD2):c.259G>A (p.Val87Ile) rs201658653
NM_006440.5(TXNRD2):c.40C>T (p.Arg14Cys) rs1259706318
NM_006440.5(TXNRD2):c.417del (p.Asn140fs) rs780054798
NM_006440.5(TXNRD2):c.497C>T (p.Thr166Met) rs553337931
NM_006440.5(TXNRD2):c.715G>A (p.Gly239Arg) rs978493213
NM_006440.5(TXNRD2):c.745C>T (p.Arg249Cys) rs557142042
NM_006440.5(TXNRD2):c.760C>T (p.Arg254Cys) rs183950022
NM_006440.5(TXNRD2):c.868G>A (p.Gly290Ser) rs777357363
NM_006440.5(TXNRD2):c.904G>A (p.Gly302Ser) rs781228620

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.