CCDC26
CCDC26 long non-coding RNA
Summary
Implicated in brain cancer and high grade glioma. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants44 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs74305956 | 8:130,377,750 | C/T | intron variant | — |
| rs10464870 | 8:130,477,823 | C/T | intron variant | — |
| rs1835842 | 8:130,478,960 | C/T | intron variant | — |
| rs113066473 | 8:130,486,415 | G/T | intron variant | — |
| rs17262815 | 8:130,491,165 | T/C | intron variant | — |
| rs891835 | 8:130,491,752 | T/G | downstream gene variant | — |
| rs10956483 | 8:130,572,110 | G/C | intron variant | — |
| rs57683624 | 8:130,590,979 | C/A | intron variant | — |
| rs7005227 | 8:130,597,858 | C/A | intron variant | — |
| rs1433578 | 8:130,601,089 | T/C | intron variant | — |
| rs2163951 | 8:130,603,357 | T/C | intron variant | — |
| rs55964818 | 8:130,605,871 | T/C | intron variant | — |
| rs12544501 | 8:130,605,931 | T/A | — | — |
| rs28500514 | 8:130,609,068 | T/C | intron variant | — |
| rs4407843 | 8:130,609,368 | A/G | — | — |
| rs2395905 | 8:130,610,739 | T/C | intron variant | — |
| rs2395906 | 8:130,610,793 | G/A | intron variant | — |
| rs10098310 | 8:130,613,614 | G/T | — | — |
| rs6989110 | 8:130,615,852 | T/A | — | — |
| rs62525615 | 8:130,618,025 | C/T | — | — |
| rs62525616 | 8:130,618,080 | C/T | — | — |
| rs59697075 | 8:130,618,150 | C/A | — | — |
| rs7341546 | 8:130,618,511 | A/T | intron variant | — |
| rs13276692 | 8:130,620,038 | G/T | intron variant | — |
| rs10956485 | 8:130,620,585 | T/C | intron variant | — |
| rs35389394 | 8:130,621,254 | C/T | intron variant | — |
| rs1991866 | 8:130,624,105 | G/A | — | — |
| rs77527100 | 8:130,626,828 | C/G | intron variant | — |
| rs16904129 | 8:130,634,936 | G/T | — | — |
| rs35823317 | 8:130,639,364 | T/A | — | — |
| rs146950370 | 8:130,641,322 | C/T | intron variant | — |
| rs6470745 | 8:130,641,921 | A/G | intron variant | — |
| rs535029080 | 8:130,644,461 | C/T | — | — |
| rs55705857 | 8:130,645,692 | A/G | intron variant | risk factor |
| rs77521439 | 8:130,657,751 | G/A | intron variant | — |
| rs62523770 | 8:130,659,170 | G/T | intron variant | — |
| rs6991966 | 8:130,673,600 | G/A | — | — |
| rs4487717 | 8:130,676,040 | C/T | intron variant | — |
| rs9918807 | 8:130,676,639 | T/C | intron variant | — |
| rs35778967 | 8:130,677,522 | T/C | intron variant | — |
| rs138628047 | 8:130,678,706 | T/C | intron variant | — |
| rs4733720 | 8:130,680,777 | C/T | — | — |
| rs4295627 | 8:130,685,457 | T/G | intron variant | — |
| rs145209947 | 8:130,694,185 | C/A | coding sequence variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.