WDR47
WD repeat domain 47
Summary
Predicted to act upstream of or within several processes, including detection of hot stimulus involved in thermoception; neuronal stem cell population maintenance; and telencephalon development. Predicted to be located in several cellular components, including growth cone; microtubule; and neuronal cell body. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants25 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2524431165 | 1:109,514,143 | T/C | — | uncertain significance |
| rs376810480 | 1:109,517,306 | G/C | — | uncertain significance |
| rs150602693 | 1:109,517,369 | T/C | — | likely benign |
| rs778118289 | 1:109,524,420 | A/G | — | uncertain significance |
| rs2524568210 | 1:109,525,293 | C/G | — | uncertain significance |
| rs1279487074 | 1:109,526,023 | T/G | — | likely pathogenic |
| rs74969346 | 1:109,527,948 | G/A | downstream gene variant | — |
| rs1425358889 | 1:109,533,899 | G/C | — | uncertain significance |
| rs140523650 | 1:109,533,937 | G/A | — | uncertain significance |
| rs1448365936 | 1:109,538,208 | C/T | — | likely benign |
| rs113434051 | 1:109,538,289 | G/A | — | uncertain significance |
| rs2524822563 | 1:109,544,895 | C/G | — | uncertain significance |
| rs2101904124 | 1:109,544,954 | T/C | — | uncertain significance |
| rs1303526940 | 1:109,547,261 | C/T | — | uncertain significance |
| rs759592678 | 1:109,547,332 | G/A | — | uncertain significance |
| rs775582082 | 1:109,553,611 | C/T | — | uncertain significance |
| rs775459672 | 1:109,553,988 | A/G | — | uncertain significance |
| rs748234241 | 1:109,554,099 | C/T | — | uncertain significance |
| rs2524961571 | 1:109,554,201 | T/C | — | uncertain significance |
| rs926474322 | 1:109,554,207 | T/C | — | uncertain significance |
| rs767448652 | 1:109,554,234 | C/T | — | uncertain significance |
| rs1417342359 | 1:109,556,479 | T/G | — | uncertain significance |
| rs140178030 | 1:109,556,543 | G/A | — | uncertain significance |
| rs184073827 | 1:109,560,146 | T/C | — | uncertain significance |
| rs778083607 | 1:109,560,197 | T/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.