LRRC34
leucine rich repeat containing 34
Summary
Predicted to be involved in cell differentiation. Predicted to act upstream of or within gene expression and telomere maintenance. Predicted to be located in cytoplasm and nucleolus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants30 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2474311631 | 3:169,511,548 | C/T | — | uncertain significance |
| rs139023558 | 3:169,511,557 | C/T | — | uncertain significance |
| rs140649463 | 3:169,511,559 | A/G | — | uncertain significance |
| rs1171891547 | 3:169,514,011 | C/T | — | uncertain significance |
| rs143470723 | 3:169,514,551 | C/T | — | uncertain significance |
| rs759141342 | 3:169,514,582 | A/G | — | uncertain significance |
| rs10936600 | 3:169,514,585 | A/C | missense variant | — |
| rs142362395 | 3:169,514,620 | C/A | — | uncertain significance |
| rs201395437 | 3:169,514,632 | G/A | — | likely benign |
| rs778622188 | 3:169,514,663 | G/A | — | uncertain significance |
| rs771955790 | 3:169,514,677 | G/A | — | uncertain significance |
| rs6793295 | 3:169,518,455 | T/G | missense variant | — |
| rs906722069 | 3:169,518,467 | G/A | — | uncertain significance |
| rs566509755 | 3:169,518,498 | G/T | — | uncertain significance |
| rs1289133836 | 3:169,518,539 | T/C | — | uncertain significance |
| rs746708653 | 3:169,521,852 | C/T | — | uncertain significance |
| rs781662061 | 3:169,521,867 | T/C | — | uncertain significance |
| rs202213975 | 3:169,521,963 | G/A | — | uncertain significance |
| rs150068897 | 3:169,524,668 | C/T | — | uncertain significance |
| rs368722671 | 3:169,525,263 | T/C | — | uncertain significance |
| rs746895981 | 3:169,525,390 | C/T | — | uncertain significance |
| rs1159226076 | 3:169,525,392 | A/T | — | likely benign |
| rs762418016 | 3:169,525,457 | G/C | — | uncertain significance |
| rs28626343 | 3:169,526,272 | T/C | intron variant | — |
| rs1347380245 | 3:169,526,418 | C/A | — | uncertain significance |
| rs747982931 | 3:169,526,464 | G/A | — | uncertain significance |
| rs1779465461 | 3:169,526,474 | T/A | — | uncertain significance |
| rs10936601 | 3:169,528,449 | C/G | — | — |
| rs1409711304 | 3:169,530,227 | G/C | — | uncertain significance |
| rs1484116096 | 3:169,530,260 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.