IL34
interleukin 34
Summary
Interleukin-34 is a cytokine that promotes the differentiation and viability of monocytes and macrophages through the colony-stimulating factor-1 receptor (CSF1R; MIM 164770) (Lin et al., 2008 [PubMed 18467591]).[supplied by OMIM, May 2008]
Known Variants34 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs554468395 | 16:70,620,879 | G/T | — | — |
| rs193281563 | 16:70,646,632 | C/T | intron variant | — |
| rs9928270 | 16:70,649,590 | G/A | intron variant | — |
| rs12928913 | 16:70,653,329 | A/T | — | — |
| rs12933193 | 16:70,653,884 | A/T | — | — |
| rs12598224 | 16:70,658,158 | G/T | intron variant | — |
| rs34538878 | 16:70,659,803 | T/C | intron variant | — |
| rs36097154 | 16:70,662,816 | G/C | — | — |
| rs71401819 | 16:70,668,385 | C/T | intron variant | — |
| rs558981823 | 16:70,672,203 | G/T | — | — |
| rs6499329 | 16:70,673,577 | T/A | — | — |
| rs12598456 | 16:70,676,478 | C/T | intron variant | — |
| rs35381200 | 16:70,677,068 | T/A | — | — |
| rs772446015 | 16:70,680,857 | C/T | — | uncertain significance |
| rs11865702 | 16:70,681,298 | A/C | — | — |
| rs34644948 | 16:70,681,658 | C/G | — | — |
| rs57752020 | 16:70,684,861 | C/G | — | — |
| rs139133476 | 16:70,688,459 | G/C | — | likely benign |
| rs1044929627 | 16:70,688,513 | A/G | — | uncertain significance |
| rs2052168113 | 16:70,688,561 | G/A | — | uncertain significance |
| rs118062333 | 16:70,690,511 | T/C | — | likely benign |
| rs779885656 | 16:70,690,565 | G/A | — | uncertain significance |
| rs78909989 | 16:70,690,858 | C/T | — | benign |
| rs780354617 | 16:70,690,910 | G/C | — | uncertain significance |
| rs2052248530 | 16:70,690,986 | G/A | — | uncertain significance |
| rs12935589 | 16:70,691,308 | C/T | downstream gene variant | — |
| rs2507097400 | 16:70,693,543 | T/C | — | uncertain significance |
| rs773227906 | 16:70,693,551 | G/A | — | uncertain significance |
| rs138898622 | 16:70,693,580 | A/G | — | benign |
| rs2507097832 | 16:70,693,586 | G/A | — | likely benign |
| rs770853044 | 16:70,693,632 | A/T | — | uncertain significance |
| rs79922158 | 16:70,693,970 | C/T | — | benign |
| rs1390364679 | 16:70,694,007 | C/T | — | uncertain significance |
| rs141513638 | 16:70,694,056 | C/T | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.