LENG9
leukocyte receptor cluster member 9
Summary
Predicted to enable zinc ion binding activity. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants42 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs7254603 | 19:54,972,719 | A/G | — | — |
| rs766173254 | 19:54,973,322 | A/G | — | likely benign |
| rs759547042 | 19:54,973,326 | G/A | — | uncertain significance |
| rs139044470 | 19:54,973,332 | G/T | — | uncertain significance |
| rs756654294 | 19:54,973,359 | C/A | — | uncertain significance |
| rs746679553 | 19:54,973,385 | A/C | — | uncertain significance |
| rs116688678 | 19:54,973,429 | G/A | — | likely benign |
| rs115358813 | 19:54,973,482 | C/T | — | uncertain significance |
| rs144970469 | 19:54,973,483 | T/G | — | uncertain significance |
| rs764496170 | 19:54,973,539 | C/G | — | uncertain significance |
| rs542592473 | 19:54,973,553 | G/A | — | uncertain significance |
| rs935120097 | 19:54,973,604 | C/T | — | uncertain significance |
| rs369115740 | 19:54,973,649 | T/G | — | likely benign |
| rs745887459 | 19:54,973,659 | C/T | — | likely benign |
| rs150136136 | 19:54,973,670 | C/A | — | likely benign |
| rs755113750 | 19:54,973,722 | C/T | — | uncertain significance |
| rs1419207456 | 19:54,973,737 | C/T | — | uncertain significance |
| rs774348441 | 19:54,973,785 | G/T | — | uncertain significance |
| rs1036658245 | 19:54,973,847 | A/T | — | uncertain significance |
| rs199881375 | 19:54,973,856 | C/G | — | uncertain significance |
| rs369858693 | 19:54,973,866 | C/T | — | uncertain significance |
| rs370733251 | 19:54,973,890 | C/T | — | uncertain significance |
| rs150665622 | 19:54,973,918 | C/A | — | likely benign |
| rs1286958831 | 19:54,973,946 | C/T | — | uncertain significance |
| rs775377747 | 19:54,974,021 | G/C | — | uncertain significance |
| rs2514691327 | 19:54,974,120 | C/T | — | uncertain significance |
| rs2514691547 | 19:54,974,159 | G/T | — | uncertain significance |
| rs748218246 | 19:54,974,180 | A/G | — | likely benign |
| rs199909342 | 19:54,974,195 | C/A | — | uncertain significance |
| rs201112601 | 19:54,974,325 | G/A | — | uncertain significance |
| rs1208481627 | 19:54,974,342 | T/G | — | uncertain significance |
| rs984550651 | 19:54,974,345 | T/G | — | uncertain significance |
| rs530528018 | 19:54,974,427 | C/G | — | uncertain significance |
| rs2514693623 | 19:54,974,445 | A/G | — | uncertain significance |
| rs2514693645 | 19:54,974,448 | C/T | — | uncertain significance |
| rs1415474246 | 19:54,974,459 | T/C | — | uncertain significance |
| rs538247982 | 19:54,974,603 | G/C | — | uncertain significance |
| rs1017542792 | 19:54,974,652 | G/A | — | uncertain significance |
| rs373014449 | 19:54,974,669 | G/T | — | uncertain significance |
| rs964655106 | 19:54,974,691 | G/A | — | uncertain significance |
| rs1026219699 | 19:54,974,708 | A/G | — | uncertain significance |
| rs1003477553 | 19:54,974,717 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.