TMEM121B
transmembrane protein 121B
Known Variants45 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs9606618 | 22:17,597,561 | G/A | downstream gene variant | — |
| rs149370082 | 22:17,600,313 | C/T | missense variant | — |
| rs2517187327 | 22:17,600,340 | C/T | — | uncertain significance |
| rs2517187364 | 22:17,600,351 | T/C | — | uncertain significance |
| rs138179417 | 22:17,600,375 | G/T | — | uncertain significance |
| rs1383742263 | 22:17,600,384 | G/A | — | uncertain significance |
| rs779538484 | 22:17,600,430 | C/G | — | uncertain significance |
| rs1049518089 | 22:17,600,454 | C/T | — | uncertain significance |
| rs771301160 | 22:17,600,456 | C/T | — | uncertain significance |
| rs753283216 | 22:17,600,589 | C/T | — | uncertain significance |
| rs371550781 | 22:17,600,683 | C/G | — | uncertain significance |
| rs1188225892 | 22:17,600,762 | G/C | — | uncertain significance |
| rs2517188662 | 22:17,600,784 | G/C | — | uncertain significance |
| rs1040909265 | 22:17,600,825 | C/T | — | uncertain significance |
| rs2517188844 | 22:17,600,852 | C/A | — | uncertain significance |
| rs1413944589 | 22:17,600,873 | G/A | — | uncertain significance |
| rs377076603 | 22:17,600,874 | G/A | — | uncertain significance |
| rs763389011 | 22:17,600,889 | G/A | — | uncertain significance |
| rs371295778 | 22:17,600,895 | C/T | — | uncertain significance |
| rs750453167 | 22:17,600,897 | C/A | — | uncertain significance |
| rs972460460 | 22:17,600,988 | G/A | — | uncertain significance |
| rs1041266243 | 22:17,601,150 | C/T | — | uncertain significance |
| rs1208670182 | 22:17,601,194 | T/G | — | uncertain significance |
| rs199862466 | 22:17,601,239 | G/A | — | uncertain significance |
| rs377534248 | 22:17,601,344 | A/G | — | uncertain significance |
| rs2061493278 | 22:17,601,390 | C/T | — | uncertain significance |
| rs746245224 | 22:17,601,443 | G/T | — | uncertain significance |
| rs768832803 | 22:17,601,456 | G/A | — | uncertain significance |
| rs561363364 | 22:17,601,470 | C/T | — | uncertain significance |
| rs1044757396 | 22:17,601,491 | C/T | — | uncertain significance |
| rs2061494296 | 22:17,601,510 | G/A | — | likely benign |
| rs1349953742 | 22:17,601,533 | G/A | — | uncertain significance |
| rs1203242383 | 22:17,601,540 | T/C | — | uncertain significance |
| rs994279888 | 22:17,601,555 | C/A | — | uncertain significance |
| rs2123827872 | 22:17,601,561 | A/C | — | uncertain significance |
| rs1268966866 | 22:17,601,638 | G/A | — | uncertain significance |
| rs897412215 | 22:17,601,740 | G/T | — | uncertain significance |
| rs888615770 | 22:17,601,816 | G/A | — | uncertain significance |
| rs1250374032 | 22:17,601,822 | C/T | — | uncertain significance |
| rs560889791 | 22:17,601,831 | C/A | — | uncertain significance |
| rs1031124100 | 22:17,601,921 | G/C | — | uncertain significance |
| rs2517192025 | 22:17,601,938 | A/C | — | uncertain significance |
| rs1418333713 | 22:17,601,945 | C/T | — | uncertain significance |
| rs1287786623 | 22:17,601,956 | G/A | — | uncertain significance |
| rs192103374 | 22:17,602,569 | C/T | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.