IL17REL
interleukin 17 receptor E like
Summary
Predicted to enable interleukin-17 receptor activity. Predicted to be involved in cytokine-mediated signaling pathway. Predicted to be located in extracellular region. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants33 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2518296113 | 22:50,435,184 | T/G | — | likely benign |
| rs541077021 | 22:50,435,197 | C/A | — | likely benign |
| rs5771069 | 22:50,435,480 | A/G | missense variant | — |
| rs751333188 | 22:50,435,786 | T/C | — | uncertain significance |
| rs1044083555 | 22:50,435,812 | C/T | — | uncertain significance |
| rs1322128131 | 22:50,435,830 | C/T | — | uncertain significance |
| rs2061043001 | 22:50,435,836 | G/T | — | uncertain significance |
| rs139236588 | 22:50,435,842 | G/A | — | uncertain significance |
| rs13054006 | 22:50,436,000 | G/C | intron variant | — |
| rs1394467999 | 22:50,436,132 | C/T | — | uncertain significance |
| rs200528585 | 22:50,436,143 | C/T | — | uncertain significance |
| rs1248963027 | 22:50,436,489 | G/A | — | uncertain significance |
| rs757387467 | 22:50,436,610 | C/T | — | likely benign |
| rs777830840 | 22:50,436,620 | C/G | — | likely benign |
| rs762312058 | 22:50,436,664 | C/T | — | likely benign |
| rs777012792 | 22:50,436,730 | C/T | — | uncertain significance |
| rs750168754 | 22:50,437,727 | A/C | — | uncertain significance |
| rs143798666 | 22:50,437,747 | G/C | — | uncertain significance |
| rs759470319 | 22:50,437,876 | G/A | — | uncertain significance |
| rs2061061131 | 22:50,437,930 | A/T | — | uncertain significance |
| rs372871983 | 22:50,438,284 | G/A | — | likely benign |
| rs370319998 | 22:50,438,344 | T/C | — | likely benign |
| rs928335507 | 22:50,438,390 | T/G | — | uncertain significance |
| rs565360497 | 22:50,439,202 | C/T | — | likely benign |
| rs376895359 | 22:50,439,241 | G/C | — | uncertain significance |
| rs758008416 | 22:50,439,283 | C/T | — | uncertain significance |
| rs757369947 | 22:50,439,290 | G/A | — | uncertain significance |
| rs749758072 | 22:50,439,531 | C/T | — | uncertain significance |
| rs754560571 | 22:50,439,537 | C/T | — | uncertain significance |
| rs773742457 | 22:50,439,549 | G/A | — | uncertain significance |
| rs140751420 | 22:50,439,585 | G/A | — | uncertain significance |
| rs753047450 | 22:50,439,609 | G/A | — | uncertain significance |
| rs4327324 | 22:50,444,649 | G/C | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.