TXNDC16
thioredoxin domain containing 16
Summary
Located in endoplasmic reticulum lumen. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants43 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs147852218 | 14:52,899,125 | A/G | — | uncertain significance |
| rs762620960 | 14:52,899,146 | G/A | — | uncertain significance |
| rs769074622 | 14:52,899,216 | T/C | — | uncertain significance |
| rs1041847901 | 14:52,899,233 | G/A | — | uncertain significance |
| rs763865016 | 14:52,899,269 | G/A | — | uncertain significance |
| rs200867005 | 14:52,899,301 | A/C | — | uncertain significance |
| rs2502718374 | 14:52,905,942 | G/A | — | uncertain significance |
| rs574451141 | 14:52,905,991 | G/T | — | uncertain significance |
| rs1002036100 | 14:52,906,017 | C/T | — | uncertain significance |
| rs61740050 | 14:52,906,042 | C/T | — | uncertain significance |
| rs748330657 | 14:52,922,094 | G/A | — | uncertain significance |
| rs139440406 | 14:52,922,151 | G/A | — | uncertain significance |
| rs981635471 | 14:52,922,163 | G/A | — | likely benign |
| rs754734150 | 14:52,923,853 | C/T | — | uncertain significance |
| rs200250325 | 14:52,923,866 | T/G | — | uncertain significance |
| rs1339297503 | 14:52,936,805 | A/G | — | likely benign |
| rs753151384 | 14:52,936,848 | C/T | — | uncertain significance |
| rs2035883402 | 14:52,937,285 | G/C | — | uncertain significance |
| rs772377428 | 14:52,937,345 | A/C | — | uncertain significance |
| rs758080672 | 14:52,937,387 | T/C | — | uncertain significance |
| rs145649990 | 14:52,937,389 | G/A | — | uncertain significance |
| rs565908826 | 14:52,948,980 | T/C | — | uncertain significance |
| rs566101143 | 14:52,949,565 | G/C | — | uncertain significance |
| rs148643190 | 14:52,949,581 | G/A | — | uncertain significance |
| rs767374230 | 14:52,949,612 | C/G | — | uncertain significance |
| rs1459607654 | 14:52,949,656 | G/C | — | uncertain significance |
| rs571400331 | 14:52,949,660 | C/T | — | uncertain significance |
| rs951010824 | 14:52,955,145 | T/G | — | uncertain significance |
| rs1354059401 | 14:52,957,701 | T/C | — | uncertain significance |
| rs10151051 | 14:52,973,316 | A/G | intron variant | — |
| rs201434300 | 14:52,977,993 | G/C | — | uncertain significance |
| rs778141797 | 14:52,978,069 | A/T | — | uncertain significance |
| rs548674668 | 14:52,978,081 | G/A | — | likely benign |
| rs145138464 | 14:52,981,650 | T/C | — | uncertain significance |
| rs775940793 | 14:52,981,665 | C/T | — | uncertain significance |
| rs1190503083 | 14:52,985,960 | C/G | — | uncertain significance |
| rs745080 | 14:52,989,228 | G/A | intron variant | — |
| rs542259575 | 14:53,003,477 | T/C | — | uncertain significance |
| rs2502958050 | 14:53,004,371 | T/C | — | uncertain significance |
| rs1322214638 | 14:53,004,383 | C/T | — | uncertain significance |
| rs774041538 | 14:53,010,164 | T/C | — | uncertain significance |
| rs370178704 | 14:53,010,188 | C/G | — | uncertain significance |
| rs374006280 | 14:53,010,197 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.