LRIG3
leucine rich repeats and immunoglobulin like domains 3
Summary
Predicted to act upstream of or within otolith morphogenesis. Located in extracellular space. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants54 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs146964202 | 12:59,266,427 | T/C | — | uncertain significance |
| rs575256838 | 12:59,266,556 | T/C | — | uncertain significance |
| rs772003425 | 12:59,267,854 | G/C | — | uncertain significance |
| rs750848857 | 12:59,267,876 | G/A | — | uncertain significance |
| rs200846498 | 12:59,268,000 | G/T | — | uncertain significance |
| rs2539644650 | 12:59,268,011 | A/T | — | uncertain significance |
| rs775913390 | 12:59,268,274 | G/A | — | uncertain significance |
| rs370313349 | 12:59,268,292 | C/T | — | uncertain significance |
| rs182093691 | 12:59,270,228 | A/T | — | likely benign |
| rs1870926438 | 12:59,270,371 | G/A | — | uncertain significance |
| rs369366724 | 12:59,271,215 | G/A | — | uncertain significance |
| rs372026653 | 12:59,271,227 | A/G | — | uncertain significance |
| rs140980524 | 12:59,271,376 | C/T | — | uncertain significance |
| rs765983743 | 12:59,271,380 | C/T | — | uncertain significance |
| rs2539648700 | 12:59,271,439 | C/A | — | uncertain significance |
| rs1236317801 | 12:59,271,473 | T/G | — | uncertain significance |
| rs2539648766 | 12:59,271,485 | A/G | — | uncertain significance |
| rs766983550 | 12:59,271,518 | C/T | — | uncertain significance |
| rs2539649048 | 12:59,271,606 | C/G | — | uncertain significance |
| rs367652315 | 12:59,271,616 | C/A | — | uncertain significance |
| rs771630854 | 12:59,271,617 | G/A | — | uncertain significance |
| rs755052796 | 12:59,272,670 | T/C | — | likely benign |
| rs777912224 | 12:59,272,699 | C/T | — | uncertain significance |
| rs2539650153 | 12:59,272,705 | A/G | — | uncertain significance |
| rs780746196 | 12:59,272,720 | C/T | — | uncertain significance |
| rs779231706 | 12:59,272,820 | C/G | — | uncertain significance |
| rs777608875 | 12:59,272,840 | C/T | — | uncertain significance |
| rs1340071028 | 12:59,272,842 | G/T | — | uncertain significance |
| rs1565614679 | 12:59,274,431 | T/C | — | uncertain significance |
| rs2539652421 | 12:59,274,500 | T/C | — | uncertain significance |
| rs768163806 | 12:59,274,507 | G/A | — | uncertain significance |
| rs371122124 | 12:59,274,581 | G/C | — | uncertain significance |
| rs142965808 | 12:59,274,638 | G/A | — | uncertain significance |
| rs1871163357 | 12:59,276,653 | C/A | — | uncertain significance |
| rs138679764 | 12:59,276,751 | C/T | — | likely benign |
| rs1358414353 | 12:59,277,335 | T/C | — | uncertain significance |
| rs1319274027 | 12:59,279,667 | C/T | — | uncertain significance |
| rs201211812 | 12:59,280,595 | C/T | — | uncertain significance |
| rs138577440 | 12:59,280,632 | T/C | — | likely benign |
| rs2539660943 | 12:59,281,599 | A/G | — | uncertain significance |
| rs1393000302 | 12:59,281,607 | T/A | — | uncertain significance |
| rs2539661712 | 12:59,282,115 | C/T | — | uncertain significance |
| rs760313447 | 12:59,282,117 | C/T | — | uncertain significance |
| rs2539661793 | 12:59,282,144 | T/A | — | uncertain significance |
| rs1264456399 | 12:59,282,145 | C/T | — | uncertain significance |
| rs777907418 | 12:59,282,743 | C/T | — | uncertain significance |
| rs144365133 | 12:59,283,829 | C/T | missense variant | — |
| rs765400991 | 12:59,283,904 | C/T | — | uncertain significance |
| rs1871405940 | 12:59,283,913 | T/C | — | uncertain significance |
| rs1481653770 | 12:59,284,463 | G/C | — | uncertain significance |
| rs757820193 | 12:59,284,538 | T/C | — | uncertain significance |
| rs1040457390 | 12:59,313,899 | C/T | — | uncertain significance |
| rs929277858 | 12:59,313,925 | C/T | — | uncertain significance |
| rs756922965 | 12:59,314,010 | C/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.