ANKRD34C
ankyrin repeat domain 34C
Summary
Predicted to be active in pi-body. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants29 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2542551942 | 15:79,585,630 | A/G | — | uncertain significance |
| rs183612932 | 15:79,585,639 | G/C | — | uncertain significance |
| rs2542552343 | 15:79,585,904 | G/C | — | uncertain significance |
| rs554040436 | 15:79,585,912 | A/G | — | uncertain significance |
| rs974198742 | 15:79,586,113 | A/G | — | uncertain significance |
| rs2542552704 | 15:79,586,162 | G/A | — | uncertain significance |
| rs1442137710 | 15:79,586,198 | T/C | — | uncertain significance |
| rs1190402936 | 15:79,586,221 | G/A | — | uncertain significance |
| rs891726268 | 15:79,586,249 | A/G | — | uncertain significance |
| rs958231841 | 15:79,586,341 | C/T | — | uncertain significance |
| rs560579919 | 15:79,586,402 | C/T | — | uncertain significance |
| rs886911869 | 15:79,586,429 | G/T | — | uncertain significance |
| rs1362116308 | 15:79,586,477 | G/A | — | uncertain significance |
| rs763799566 | 15:79,586,516 | C/G | — | uncertain significance |
| rs1039697550 | 15:79,586,526 | C/G | — | uncertain significance |
| rs199526749 | 15:79,586,737 | T/C | — | uncertain significance |
| rs2542553648 | 15:79,586,741 | T/A | — | uncertain significance |
| rs1190360690 | 15:79,586,765 | A/G | — | uncertain significance |
| rs774762530 | 15:79,586,767 | G/C | — | uncertain significance |
| rs990335513 | 15:79,586,778 | A/G | — | uncertain significance |
| rs2542553734 | 15:79,586,783 | C/T | — | uncertain significance |
| rs759077946 | 15:79,586,806 | A/T | — | uncertain significance |
| rs569161480 | 15:79,586,939 | C/T | — | uncertain significance |
| rs952337784 | 15:79,587,025 | A/C | — | uncertain significance |
| rs984065205 | 15:79,587,034 | C/A | — | uncertain significance |
| rs544010032 | 15:79,587,041 | C/T | — | uncertain significance |
| rs557571456 | 15:79,587,091 | A/G | — | uncertain significance |
| rs772285559 | 15:79,587,106 | A/G | — | uncertain significance |
| rs932758594 | 15:79,587,109 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.