TXNDC11
thioredoxin domain containing 11
Summary
Predicted to be located in endoplasmic reticulum membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants71 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs762745074 | 16:11,773,074 | T/C | — | uncertain significance |
| rs139507945 | 16:11,773,089 | G/T | — | uncertain significance |
| rs146844027 | 16:11,773,166 | T/A | — | uncertain significance |
| rs2050345324 | 16:11,773,172 | T/C | — | uncertain significance |
| rs570323012 | 16:11,773,184 | G/T | — | uncertain significance |
| rs151281237 | 16:11,773,230 | T/A | — | uncertain significance |
| rs8191350 | 16:11,773,261 | G/C | — | benign |
| rs2548315660 | 16:11,773,283 | T/C | — | uncertain significance |
| rs1278059856 | 16:11,773,293 | C/T | — | uncertain significance |
| rs765045815 | 16:11,773,354 | C/G | — | uncertain significance |
| rs561506406 | 16:11,773,368 | C/T | — | likely benign |
| rs766106740 | 16:11,773,479 | G/A | — | uncertain significance |
| rs767623872 | 16:11,773,484 | C/T | — | uncertain significance |
| rs1293111741 | 16:11,773,551 | C/T | — | uncertain significance |
| rs760644439 | 16:11,773,583 | T/C | — | uncertain significance |
| rs2548316879 | 16:11,773,643 | T/C | — | uncertain significance |
| rs2141964882 | 16:11,778,031 | G/A | — | uncertain significance |
| rs11639651 | 16:11,781,260 | G/A | intron variant | — |
| rs79362431 | 16:11,781,741 | G/C | — | likely benign |
| rs61739869 | 16:11,781,790 | G/A | — | benign |
| rs61739865 | 16:11,781,802 | G/A | — | benign |
| rs199732787 | 16:11,782,223 | G/A | — | uncertain significance |
| rs1211112871 | 16:11,782,275 | G/A | — | uncertain significance |
| rs534755544 | 16:11,785,151 | G/A | — | uncertain significance |
| rs905813417 | 16:11,785,176 | G/C | — | uncertain significance |
| rs772194843 | 16:11,785,207 | G/T | — | uncertain significance |
| rs2548331973 | 16:11,785,214 | A/G | — | uncertain significance |
| rs1019998000 | 16:11,785,233 | C/T | — | uncertain significance |
| rs1204190402 | 16:11,785,281 | A/T | — | uncertain significance |
| rs1597415039 | 16:11,785,297 | G/A | — | likely benign |
| rs772846078 | 16:11,785,401 | C/T | — | likely benign |
| rs950120333 | 16:11,785,407 | T/C | — | uncertain significance |
| rs1004860034 | 16:11,785,491 | A/C | — | uncertain significance |
| rs759825009 | 16:11,785,572 | A/T | — | uncertain significance |
| rs2548333362 | 16:11,785,674 | C/T | — | uncertain significance |
| rs748377323 | 16:11,785,775 | C/T | — | uncertain significance |
| rs748428736 | 16:11,785,800 | G/A | — | uncertain significance |
| rs779006508 | 16:11,785,860 | C/T | — | uncertain significance |
| rs773301942 | 16:11,785,866 | G/A | — | uncertain significance |
| rs561326612 | 16:11,785,883 | C/T | — | uncertain significance |
| rs376827908 | 16:11,785,884 | G/A | — | uncertain significance |
| rs144296098 | 16:11,785,886 | T/A | — | uncertain significance |
| rs754173608 | 16:11,785,901 | C/G | — | uncertain significance |
| rs758339345 | 16:11,785,932 | C/T | — | uncertain significance |
| rs35722622 | 16:11,787,689 | C/A | intron variant | — |
| rs143169078 | 16:11,792,004 | C/T | — | uncertain significance |
| rs370268157 | 16:11,792,039 | G/A | — | uncertain significance |
| rs201331028 | 16:11,792,094 | G/A | — | uncertain significance |
| rs746235924 | 16:11,794,351 | T/C | — | uncertain significance |
| rs1323818485 | 16:11,794,364 | C/A | — | uncertain significance |
| rs4584833 | 16:11,798,758 | C/G | — | — |
| rs534644417 | 16:11,815,468 | G/A | — | uncertain significance |
| rs749070937 | 16:11,824,571 | C/T | — | uncertain significance |
| rs1018992335 | 16:11,824,611 | T/C | — | uncertain significance |
| rs570693250 | 16:11,824,617 | C/T | — | uncertain significance |
| rs2548383535 | 16:11,827,857 | T/G | — | uncertain significance |
| rs779959265 | 16:11,827,877 | T/C | — | uncertain significance |
| rs1017040573 | 16:11,827,895 | T/G | — | uncertain significance |
| rs2548383648 | 16:11,827,922 | G/A | — | uncertain significance |
| rs140374310 | 16:11,829,886 | C/T | — | likely benign |
| rs953784701 | 16:11,830,016 | G/C | — | uncertain significance |
| rs149715115 | 16:11,830,055 | G/A | — | uncertain significance |
| rs1055468040 | 16:11,836,351 | G/A | — | uncertain significance |
| rs1420003794 | 16:11,836,358 | G/A | — | uncertain significance |
| rs552851178 | 16:11,836,378 | A/G | — | uncertain significance |
| rs999610009 | 16:11,836,396 | T/G | — | uncertain significance |
| rs966264167 | 16:11,836,411 | G/A | — | uncertain significance |
| rs531792677 | 16:11,836,421 | A/G | — | uncertain significance |
| rs961878540 | 16:11,836,494 | G/C | — | uncertain significance |
| rs781662574 | 16:11,836,523 | C/T | — | uncertain significance |
| rs377313827 | 16:11,836,568 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.