WDR89
WD repeat domain 89
Summary
Predicted to act upstream of or within corpus callosum development and ventricular system development. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants39 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs576477902 | 14:64,065,540 | C/T | — | uncertain significance |
| rs138166073 | 14:64,065,556 | C/T | — | uncertain significance |
| rs571324018 | 14:64,065,600 | T/C | — | uncertain significance |
| rs2549452313 | 14:64,065,635 | A/T | — | uncertain significance |
| rs188415224 | 14:64,065,687 | C/T | — | uncertain significance |
| rs1201830923 | 14:64,065,694 | T/C | — | uncertain significance |
| rs541626796 | 14:64,065,742 | T/C | — | uncertain significance |
| rs1894921337 | 14:64,065,798 | G/A | — | uncertain significance |
| rs1212119686 | 14:64,065,804 | G/C | — | uncertain significance |
| rs1894924654 | 14:64,065,837 | T/C | — | uncertain significance |
| rs775316974 | 14:64,065,891 | C/T | — | uncertain significance |
| rs767911526 | 14:64,065,954 | G/A | — | uncertain significance |
| rs772710618 | 14:64,066,066 | C/T | — | uncertain significance |
| rs749358111 | 14:64,066,173 | C/A | — | uncertain significance |
| rs182117567 | 14:64,066,230 | A/C | — | uncertain significance |
| rs148702795 | 14:64,066,253 | T/A | — | uncertain significance |
| rs762450286 | 14:64,066,315 | T/C | — | uncertain significance |
| rs1262476077 | 14:64,066,354 | T/C | — | uncertain significance |
| rs778748751 | 14:64,066,510 | A/G | — | uncertain significance |
| rs746532791 | 14:64,066,548 | C/A | — | uncertain significance |
| rs61984031 | 14:64,071,096 | A/T | downstream gene variant | — |
| rs61984033 | 14:64,071,999 | C/A | regulatory region variant | — |
| rs61984036 | 14:64,075,331 | A/C | intron variant | — |
| rs116977984 | 14:64,077,953 | G/C | intron variant | — |
| rs118069495 | 14:64,080,637 | G/C | upstream gene variant | — |
| rs184813771 | 14:64,083,248 | C/T | upstream gene variant | — |
| rs61984044 | 14:64,095,505 | C/T | upstream gene variant | — |
| rs61984045 | 14:64,095,514 | A/G | upstream gene variant | — |
| rs61984047 | 14:64,099,078 | A/G | downstream gene variant | — |
| rs61984048 | 14:64,099,387 | T/G | downstream gene variant | — |
| rs8020833 | 14:64,105,408 | A/G | intron variant | — |
| rs55665448 | 14:64,106,415 | C/A | — | — |
| rs61984055 | 14:64,106,929 | G/A | intron variant | — |
| rs73263634 | 14:64,107,656 | A/G | intron variant | — |
| rs8018194 | 14:64,108,348 | G/C | regulatory region variant | — |
| rs8018382 | 14:64,108,454 | G/C | regulatory region variant | — |
| rs61985669 | 14:64,108,582 | A/C | regulatory region variant | — |
| rs8018872 | 14:64,108,884 | C/T | regulatory region variant | — |
| rs56060943 | 14:64,110,437 | G/A | upstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.