TMEM169
transmembrane protein 169
Summary
Predicted to be located in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants28 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2469247503 | 2:216,960,737 | C/A | — | uncertain significance |
| rs140150309 | 2:216,960,759 | G/A | — | uncertain significance |
| rs200022914 | 2:216,960,775 | C/T | — | uncertain significance |
| rs138032584 | 2:216,960,801 | C/T | — | uncertain significance |
| rs369348749 | 2:216,960,805 | G/A | — | uncertain significance |
| rs372176280 | 2:216,960,852 | C/G | — | uncertain significance |
| rs143856543 | 2:216,960,853 | G/T | — | uncertain significance |
| rs374430787 | 2:216,960,885 | G/A | — | uncertain significance |
| rs2469248195 | 2:216,960,951 | G/A | — | uncertain significance |
| rs377120029 | 2:216,964,666 | A/G | — | uncertain significance |
| rs143173919 | 2:216,964,700 | G/A | — | uncertain significance |
| rs2469253334 | 2:216,964,709 | A/G | — | uncertain significance |
| rs1696354337 | 2:216,964,807 | G/A | — | uncertain significance |
| rs766422942 | 2:216,964,816 | G/C | — | uncertain significance |
| rs755117065 | 2:216,964,862 | C/A | — | uncertain significance |
| rs1696363453 | 2:216,965,014 | C/T | — | uncertain significance |
| rs747642228 | 2:216,965,017 | G/T | — | uncertain significance |
| rs368056286 | 2:216,965,025 | C/G | — | uncertain significance |
| rs779968539 | 2:216,965,075 | C/T | — | uncertain significance |
| rs142981658 | 2:216,965,100 | A/T | — | uncertain significance |
| rs140200885 | 2:216,965,110 | G/A | — | uncertain significance |
| rs1288365799 | 2:216,965,113 | A/G | — | uncertain significance |
| rs1696369048 | 2:216,965,119 | A/G | — | uncertain significance |
| rs1559230462 | 2:216,965,123 | G/C | — | uncertain significance |
| rs201189708 | 2:216,965,214 | C/G | — | uncertain significance |
| rs754761398 | 2:216,965,222 | C/G | — | uncertain significance |
| rs758398610 | 2:216,965,234 | C/G | — | uncertain significance |
| rs142015527 | 2:216,965,258 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.