TMEM132D
transmembrane protein 132D
Summary
Predicted to be located in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants121 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs776455207 | 12:129,558,433 | T/C | — | likely benign |
| rs759382977 | 12:129,558,446 | T/C | — | uncertain significance |
| rs758753338 | 12:129,558,462 | T/C | — | likely benign |
| rs764238814 | 12:129,558,465 | G/A | — | likely benign |
| rs1593250509 | 12:129,558,473 | C/T | — | uncertain significance |
| rs1242467133 | 12:129,558,494 | C/A | — | uncertain significance |
| rs370402247 | 12:129,558,503 | T/C | — | uncertain significance |
| rs749663236 | 12:129,558,512 | C/T | — | uncertain significance |
| rs770396800 | 12:129,558,524 | C/T | — | uncertain significance |
| rs74344050 | 12:129,558,537 | A/G | — | benign |
| rs74724941 | 12:129,558,549 | G/A | — | benign |
| rs143281224 | 12:129,558,566 | C/T | — | likely benign |
| rs2135601686 | 12:129,558,605 | T/C | — | uncertain significance |
| rs199691995 | 12:129,558,717 | T/C | — | likely benign |
| rs77652071 | 12:129,558,761 | G/C | — | uncertain significance |
| rs1401283585 | 12:129,558,967 | A/G | — | uncertain significance |
| rs138024935 | 12:129,559,045 | A/T | — | uncertain significance |
| rs200821494 | 12:129,559,060 | C/T | — | uncertain significance |
| rs150964423 | 12:129,559,063 | G/T | — | benign |
| rs202155136 | 12:129,559,082 | T/A | — | uncertain significance |
| rs555131 | 12:129,559,086 | A/C | — | benign |
| rs751535148 | 12:129,559,110 | G/C | — | uncertain significance |
| rs142956798 | 12:129,559,175 | G/A | — | uncertain significance |
| rs140762080 | 12:129,559,228 | G/A | — | benign |
| rs143905056 | 12:129,559,231 | G/A | — | uncertain significance |
| rs971265703 | 12:129,559,243 | C/T | — | uncertain significance |
| rs981706165 | 12:129,559,258 | T/C | — | uncertain significance |
| rs760498916 | 12:129,559,301 | T/C | — | uncertain significance |
| rs372639691 | 12:129,559,335 | A/G | — | likely benign |
| rs1244480082 | 12:129,559,397 | C/T | — | uncertain significance |
| rs73159540 | 12:129,559,421 | C/T | — | benign |
| rs10773594 | 12:129,559,557 | C/T | — | benign |
| rs12369635 | 12:129,561,356 | C/A | — | — |
| rs1380549375 | 12:129,563,102 | C/T | — | uncertain significance |
| rs2541193283 | 12:129,563,215 | T/C | — | uncertain significance |
| rs371664509 | 12:129,566,348 | C/T | — | uncertain significance |
| rs184530178 | 12:129,566,386 | A/G | — | uncertain significance |
| rs759077899 | 12:129,566,452 | C/T | — | uncertain significance |
| rs758174835 | 12:129,566,462 | C/T | — | uncertain significance |
| rs770577561 | 12:129,566,498 | C/G | — | uncertain significance |
| rs1458505012 | 12:129,566,507 | G/A | — | uncertain significance |
| rs550150452 | 12:129,566,551 | T/G | — | uncertain significance |
| rs1442103827 | 12:129,566,555 | C/T | — | uncertain significance |
| rs144217964 | 12:129,566,566 | C/T | — | likely benign |
| rs367939457 | 12:129,566,571 | G/A | — | likely benign |
| rs766678401 | 12:129,569,061 | G/A | — | uncertain significance |
| rs929464545 | 12:129,569,063 | A/G | — | uncertain significance |
| rs528294635 | 12:129,569,092 | G/A | — | likely benign |
| rs565021234 | 12:129,569,107 | G/A | — | likely benign |
| rs369239393 | 12:129,569,123 | C/T | — | uncertain significance |
| rs144267550 | 12:129,569,124 | G/A | — | uncertain significance |
| rs1333673533 | 12:129,569,168 | T/G | — | uncertain significance |
| rs757602371 | 12:129,569,185 | C/T | — | likely benign |
| rs767934327 | 12:129,569,187 | C/T | — | uncertain significance |
| rs148352740 | 12:129,569,226 | C/T | — | uncertain significance |
| rs2135620101 | 12:129,569,241 | C/G | — | uncertain significance |
| rs12824981 | 12:129,637,348 | C/T | regulatory region variant | — |
| rs12580240 | 12:129,646,572 | A/G | intron variant | — |
| rs12580533 | 12:129,646,601 | T/C | intron variant | — |
| rs762639339 | 12:129,694,059 | A/G | — | likely benign |
| rs756867549 | 12:129,694,073 | C/T | — | uncertain significance |
| rs145352969 | 12:129,694,074 | G/A | — | likely benign |
| rs1244496092 | 12:129,694,108 | A/G | — | uncertain significance |
| rs1410065607 | 12:129,694,127 | C/T | — | uncertain significance |
| rs150876325 | 12:129,694,155 | C/T | — | likely benign |
| rs771427502 | 12:129,694,177 | G/A | — | uncertain significance |
| rs12816732 | 12:129,694,206 | C/T | — | benign |
| rs750542701 | 12:129,822,193 | C/A | — | uncertain significance |
| rs780735174 | 12:129,822,201 | A/G | — | uncertain significance |
| rs1271494578 | 12:129,822,249 | G/A | — | uncertain significance |
| rs775335868 | 12:129,822,254 | C/G | — | likely benign |
| rs2541427808 | 12:129,822,288 | T/G | — | uncertain significance |
| rs201444385 | 12:129,822,304 | C/T | — | uncertain significance |
| rs754370941 | 12:129,822,312 | T/C | — | uncertain significance |
| rs775490465 | 12:129,822,354 | C/T | — | uncertain significance |
| rs149909262 | 12:129,822,358 | C/T | — | uncertain significance |
| rs111638979 | 12:129,889,219 | G/A | intron variant | — |
| rs7309727 | 12:129,955,359 | T/C | intron variant | — |
| rs11060369 | 12:129,960,197 | A/C | intron variant | — |
| rs760922461 | 12:130,015,617 | C/T | — | uncertain significance |
| rs144926631 | 12:130,015,620 | C/G | — | likely benign |
| rs148665372 | 12:130,015,672 | C/T | — | likely benign |
| rs116456206 | 12:130,015,673 | G/T | — | uncertain significance |
| rs772149560 | 12:130,015,677 | G/A | — | uncertain significance |
| rs759524697 | 12:130,015,712 | C/T | — | uncertain significance |
| rs141468212 | 12:130,015,720 | G/A | — | likely benign |
| rs155370 | 12:130,077,096 | T/C | — | association |
| rs114606502 | 12:130,117,352 | T/C | intron variant | — |
| rs1881332562 | 12:130,184,361 | G/T | — | uncertain significance |
| rs553796623 | 12:130,184,413 | C/T | — | uncertain significance |
| rs184778944 | 12:130,184,429 | G/A | — | likely benign |
| rs762633426 | 12:130,184,531 | C/A | — | uncertain significance |
| rs2541392659 | 12:130,184,533 | A/T | — | uncertain significance |
| rs750383951 | 12:130,184,542 | C/T | — | uncertain significance |
| rs1253234057 | 12:130,184,551 | C/T | — | uncertain significance |
| rs76591377 | 12:130,184,594 | G/A | — | benign |
| rs1194795519 | 12:130,184,601 | C/T | — | likely benign |
| rs2137226130 | 12:130,184,661 | C/T | — | uncertain significance |
| rs372463803 | 12:130,184,705 | G/T | — | likely benign |
| rs141605203 | 12:130,184,710 | G/T | — | uncertain significance |
Showing 100 of 121 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.