LRRC49
leucine rich repeat containing 49
Summary
Located in centriolar satellite. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants35 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs751297011 | 15:71,185,268 | G/A | — | uncertain significance |
| rs780001983 | 15:71,188,248 | C/G | — | uncertain significance |
| rs773996221 | 15:71,193,267 | A/G | — | uncertain significance |
| rs149347450 | 15:71,193,350 | T/A | — | uncertain significance |
| rs533422376 | 15:71,195,901 | A/T | — | — |
| rs2034222096 | 15:71,196,941 | T/C | — | uncertain significance |
| rs779422521 | 15:71,196,971 | G/A | — | uncertain significance |
| rs2505738414 | 15:71,196,998 | A/C | — | uncertain significance |
| rs772445452 | 15:71,203,879 | A/C | — | uncertain significance |
| rs2505767182 | 15:71,211,504 | A/C | — | uncertain significance |
| rs558846231 | 15:71,224,153 | G/A | — | — |
| rs745785612 | 15:71,256,181 | T/A | — | uncertain significance |
| rs776104198 | 15:71,256,236 | A/G | — | uncertain significance |
| rs373589573 | 15:71,256,246 | G/A | — | uncertain significance |
| rs753124747 | 15:71,256,270 | C/T | — | uncertain significance |
| rs754131524 | 15:71,272,452 | C/T | — | uncertain significance |
| rs189232824 | 15:71,272,458 | G/A | — | uncertain significance |
| rs1457514278 | 15:71,272,494 | C/T | — | uncertain significance |
| rs149661179 | 15:71,276,530 | C/T | — | uncertain significance |
| rs146676391 | 15:71,276,555 | G/T | — | uncertain significance |
| rs75464765 | 15:71,283,997 | G/A | intron variant | — |
| rs1438318233 | 15:71,300,723 | T/C | — | uncertain significance |
| rs748724167 | 15:71,300,738 | A/G | — | uncertain significance |
| rs1174871782 | 15:71,300,864 | G/A | — | uncertain significance |
| rs376633327 | 15:71,300,911 | G/A | — | uncertain significance |
| rs2505922682 | 15:71,302,198 | T/C | — | uncertain significance |
| rs570407752 | 15:71,302,209 | C/T | — | uncertain significance |
| rs569228547 | 15:71,302,236 | C/G | — | uncertain significance |
| rs1372600330 | 15:71,302,326 | A/C | — | uncertain significance |
| rs201689534 | 15:71,305,159 | T/C | — | uncertain significance |
| rs200517146 | 15:71,305,227 | C/G | — | uncertain significance |
| rs747780669 | 15:71,329,527 | A/T | — | uncertain significance |
| rs375232495 | 15:71,329,578 | A/C | — | uncertain significance |
| rs747525856 | 15:71,329,655 | A/G | — | uncertain significance |
| rs369564990 | 15:71,341,814 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.