TMEM176B
transmembrane protein 176B
Summary
Predicted to be involved in negative regulation of dendritic cell differentiation. Predicted to be located in nuclear membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants22 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs770643397 | 7:150,489,214 | T/C | — | uncertain significance |
| rs138108608 | 7:150,489,244 | C/A | — | uncertain significance |
| rs139047290 | 7:150,489,245 | G/T | — | uncertain significance |
| rs199899772 | 7:150,489,247 | A/G | — | uncertain significance |
| rs1300336890 | 7:150,490,183 | A/G | — | uncertain significance |
| rs750841048 | 7:150,490,190 | T/A | — | uncertain significance |
| rs939615418 | 7:150,490,213 | T/G | — | uncertain significance |
| rs772939068 | 7:150,490,234 | C/T | — | likely benign |
| rs1563030667 | 7:150,490,256 | T/C | — | uncertain significance |
| rs202026562 | 7:150,490,345 | A/G | — | uncertain significance |
| rs770220387 | 7:150,491,083 | C/T | — | uncertain significance |
| rs2485730818 | 7:150,491,140 | C/T | — | uncertain significance |
| rs546782372 | 7:150,493,501 | T/C | — | uncertain significance |
| rs140393291 | 7:150,493,503 | T/A | — | uncertain significance |
| rs1798526772 | 7:150,493,506 | C/T | — | uncertain significance |
| rs1418923415 | 7:150,493,524 | T/C | — | uncertain significance |
| rs2485748098 | 7:150,493,587 | T/G | — | uncertain significance |
| rs373657332 | 7:150,493,623 | G/A | — | uncertain significance |
| rs1451753088 | 7:150,493,630 | C/T | — | uncertain significance |
| rs115946508 | 7:150,497,496 | C/A | regulatory region variant | — |
| rs1108578 | 7:150,498,508 | G/T | regulatory region variant | — |
| rs714885 | 7:150,499,787 | T/G | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.