NOL4
nucleolar protein 4
Summary
Predicted to enable RNA binding activity. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants31 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs140091305 | 18:31,432,966 | G/A | — | uncertain significance |
| rs186886637 | 18:31,461,953 | A/T | intron variant | — |
| rs972609703 | 18:31,463,315 | G/A | — | uncertain significance |
| rs911052958 | 18:31,463,349 | C/T | — | uncertain significance |
| rs34755825 | 18:31,494,617 | A/T | regulatory region variant | — |
| rs149780392 | 18:31,500,154 | G/A | intron variant | — |
| rs370304044 | 18:31,523,046 | G/A | — | uncertain significance |
| rs17747791 | 18:31,531,765 | T/A | intron variant | — |
| rs201753634 | 18:31,538,240 | G/A | — | uncertain significance |
| rs898390036 | 18:31,538,376 | C/T | — | uncertain significance |
| rs7240554 | 18:31,566,142 | T/C | intron variant | — |
| rs140336684 | 18:31,570,017 | T/A | intron variant | — |
| rs1941348 | 18:31,572,531 | C/A | intron variant | — |
| rs953322978 | 18:31,599,307 | C/T | — | uncertain significance |
| rs1387546446 | 18:31,599,308 | G/C | — | uncertain significance |
| rs773755694 | 18:31,599,328 | A/G | — | uncertain significance |
| rs749002031 | 18:31,599,377 | T/C | — | uncertain significance |
| rs369453065 | 18:31,599,386 | C/G | — | uncertain significance |
| rs772761092 | 18:31,599,391 | G/A | — | uncertain significance |
| rs8083926 | 18:31,606,828 | C/G | intron variant | — |
| rs7239368 | 18:31,645,379 | G/C | — | — |
| rs4239386 | 18:31,664,710 | T/A | intron variant | — |
| rs370334753 | 18:31,673,549 | T/C | — | uncertain significance |
| rs537993787 | 18:31,709,947 | C/T | — | uncertain significance |
| rs755854498 | 18:31,709,948 | G/A | — | uncertain significance |
| rs9944701 | 18:31,743,309 | C/T | — | — |
| rs759309117 | 18:31,802,955 | G/A | — | uncertain significance |
| rs781459896 | 18:31,802,994 | C/A | — | uncertain significance |
| rs746220512 | 18:31,802,995 | C/A | — | uncertain significance |
| rs376462407 | 18:31,803,084 | G/A | — | uncertain significance |
| rs185815640 | 18:31,803,096 | T/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.