TMEM178B
transmembrane protein 178B
Summary
Predicted to be active in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants16 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2535656961 | 7:140,774,118 | C/T | — | uncertain significance |
| rs970027767 | 7:140,774,197 | C/A | — | uncertain significance |
| rs1210791994 | 7:140,774,198 | C/T | — | uncertain significance |
| rs766863820 | 7:140,774,352 | G/C | — | uncertain significance |
| rs749990889 | 7:140,774,478 | C/T | — | uncertain significance |
| rs144433643 | 7:140,846,673 | G/C | — | — |
| rs374826641 | 7:140,860,679 | C/T | — | — |
| rs16882396 | 7:140,888,321 | C/G | intron variant | — |
| rs1049056387 | 7:140,912,481 | G/A | — | uncertain significance |
| rs2535803774 | 7:140,912,491 | G/C | — | uncertain significance |
| rs7809517 | 7:140,914,456 | A/G | intron variant | — |
| rs2159759 | 7:140,916,466 | A/T | — | — |
| rs776267447 | 7:141,137,445 | G/A | — | likely benign |
| rs1037708144 | 7:141,137,491 | T/C | — | uncertain significance |
| rs1382629290 | 7:141,170,473 | G/A | — | uncertain significance |
| rs757257299 | 7:141,170,537 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.