LRRC1
leucine rich repeat containing 1
Summary
Located in cytosol. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants30 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs34113003 | 6:53,659,234 | C/T | regulatory region variant | — |
| rs201594887 | 6:53,660,086 | A/G | — | uncertain significance |
| rs61737021 | 6:53,660,101 | G/T | — | benign |
| rs1764261293 | 6:53,660,158 | C/T | — | uncertain significance |
| rs139603931 | 6:53,693,025 | A/G | intron variant | — |
| rs368836742 | 6:53,706,983 | G/T | — | uncertain significance |
| rs115880839 | 6:53,736,488 | G/A | intron variant | — |
| rs762673828 | 6:53,743,812 | G/T | — | uncertain significance |
| rs2481376996 | 6:53,761,661 | G/A | — | uncertain significance |
| rs748962882 | 6:53,764,565 | C/A | — | uncertain significance |
| rs200231839 | 6:53,764,585 | C/G | — | uncertain significance |
| rs1229891452 | 6:53,764,594 | G/A | — | uncertain significance |
| rs372298061 | 6:53,767,432 | C/G | — | uncertain significance |
| rs763233291 | 6:53,767,493 | T/C | — | uncertain significance |
| rs1173599741 | 6:53,767,505 | A/G | — | uncertain significance |
| rs769808539 | 6:53,769,193 | T/C | — | uncertain significance |
| rs2481395506 | 6:53,769,233 | A/C | — | uncertain significance |
| rs886834828 | 6:53,778,658 | G/A | — | uncertain significance |
| rs1211824451 | 6:53,778,700 | C/A | — | uncertain significance |
| rs200438450 | 6:53,778,707 | G/A | — | uncertain significance |
| rs180993604 | 6:53,784,313 | T/C | — | uncertain significance |
| rs768447766 | 6:53,784,463 | G/C | — | uncertain significance |
| rs772638013 | 6:53,785,431 | C/T | — | uncertain significance |
| rs760325227 | 6:53,785,465 | A/G | — | uncertain significance |
| rs775316563 | 6:53,785,524 | G/A | — | uncertain significance |
| rs765376240 | 6:53,787,449 | G/A | — | uncertain significance |
| rs750579414 | 6:53,787,480 | C/G | — | uncertain significance |
| rs538702416 | 6:53,787,505 | C/T | — | uncertain significance |
| rs761915713 | 6:53,787,550 | G/A | — | uncertain significance |
| rs61734465 | 6:53,787,585 | T/G | — | benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.