TMEM132B
transmembrane protein 132B
Summary
Predicted to be located in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants67 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs146549691 | 12:125,672,490 | T/C | intron variant | — |
| rs1571885 | 12:125,674,490 | A/G | intron variant | — |
| rs326391 | 12:125,806,227 | C/A | — | — |
| rs1876580843 | 12:125,811,203 | G/T | — | likely benign |
| rs199619853 | 12:125,811,219 | G/A | — | uncertain significance |
| rs772736831 | 12:125,834,043 | C/T | — | uncertain significance |
| rs2541744672 | 12:125,834,049 | C/G | — | uncertain significance |
| rs369832413 | 12:125,834,081 | A/G | — | likely benign |
| rs200926788 | 12:125,834,111 | G/A | — | uncertain significance |
| rs1227597402 | 12:125,834,157 | A/C | — | uncertain significance |
| rs766246833 | 12:125,834,186 | C/G | — | uncertain significance |
| rs755160116 | 12:125,834,187 | C/A | — | uncertain significance |
| rs2541745193 | 12:125,834,207 | T/C | — | uncertain significance |
| rs1352101057 | 12:125,834,231 | A/T | — | uncertain significance |
| rs751624463 | 12:125,834,280 | A/G | — | uncertain significance |
| rs369009903 | 12:125,834,468 | C/T | — | uncertain significance |
| rs917663571 | 12:125,834,529 | G/A | — | uncertain significance |
| rs370220788 | 12:125,834,586 | C/T | — | uncertain significance |
| rs201217999 | 12:125,834,604 | C/T | — | uncertain significance |
| rs2541746713 | 12:125,834,691 | C/T | — | uncertain significance |
| rs369457906 | 12:125,834,696 | C/A | — | uncertain significance |
| rs772168951 | 12:125,834,762 | T/C | — | uncertain significance |
| rs746736412 | 12:125,834,783 | G/A | — | uncertain significance |
| rs138362432 | 12:125,834,799 | C/T | — | uncertain significance |
| rs866219544 | 12:125,834,831 | A/G | — | uncertain significance |
| rs747888388 | 12:125,834,832 | C/T | — | uncertain significance |
| rs1147246 | 12:125,875,466 | T/G | intron variant | — |
| rs776383335 | 12:125,900,109 | C/T | — | uncertain significance |
| rs939836559 | 12:125,900,139 | C/A | — | uncertain significance |
| rs201518513 | 12:125,900,175 | C/T | — | uncertain significance |
| rs781241046 | 12:125,900,178 | C/T | — | uncertain significance |
| rs769230508 | 12:125,900,207 | C/G | — | uncertain significance |
| rs35052438 | 12:125,911,391 | C/G | intron variant | — |
| rs2542211670 | 12:126,003,993 | G/T | — | uncertain significance |
| rs368219345 | 12:126,004,049 | G/T | — | uncertain significance |
| rs199663478 | 12:126,004,148 | G/A | — | uncertain significance |
| rs142261172 | 12:126,049,981 | G/A | intron variant | — |
| rs761009186 | 12:126,068,460 | G/A | — | uncertain significance |
| rs202118018 | 12:126,068,490 | G/T | — | uncertain significance |
| rs199976507 | 12:126,068,523 | G/A | — | uncertain significance |
| rs754898198 | 12:126,128,649 | G/A | — | uncertain significance |
| rs778033275 | 12:126,128,683 | C/T | — | uncertain significance |
| rs2541762907 | 12:126,128,794 | A/G | — | uncertain significance |
| rs10846938 | 12:126,130,562 | G/T | intron variant | — |
| rs758736045 | 12:126,135,290 | C/A | — | uncertain significance |
| rs371149663 | 12:126,135,311 | C/T | — | uncertain significance |
| rs377328783 | 12:126,135,430 | G/C | — | uncertain significance |
| rs753441483 | 12:126,135,440 | G/A | — | uncertain significance |
| rs200968619 | 12:126,135,455 | G/A | — | uncertain significance |
| rs16919359 | 12:126,137,060 | C/T | — | benign |
| rs762647711 | 12:126,137,090 | T/C | — | uncertain significance |
| rs1406947998 | 12:126,137,108 | C/T | — | uncertain significance |
| rs2541779397 | 12:126,137,111 | A/G | — | uncertain significance |
| rs772753714 | 12:126,138,142 | G/A | — | uncertain significance |
| rs759478360 | 12:126,138,166 | A/C | — | uncertain significance |
| rs867174287 | 12:126,138,286 | G/A | — | uncertain significance |
| rs762724698 | 12:126,138,310 | T/C | — | uncertain significance |
| rs780660903 | 12:126,138,400 | A/T | — | uncertain significance |
| rs185856785 | 12:126,138,454 | A/G | — | uncertain significance |
| rs757921642 | 12:126,138,477 | C/T | — | uncertain significance |
| rs376218579 | 12:126,138,498 | G/A | — | uncertain significance |
| rs776799042 | 12:126,138,549 | A/G | — | uncertain significance |
| rs747184399 | 12:126,138,659 | C/A | — | likely benign |
| rs775624808 | 12:126,138,834 | A/G | — | uncertain significance |
| rs2541784646 | 12:126,138,878 | A/T | — | uncertain significance |
| rs1593049305 | 12:126,138,981 | A/G | — | likely benign |
| rs1043607 | 12:126,143,346 | G/A | 3 prime UTR variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.