LCORL
ligand dependent nuclear receptor corepressor like
Summary
This gene encodes a transcription factor that appears to function in spermatogenesis. Polymorphisms in this gene are associated with measures of skeletal frame size and adult height. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]
Known Variants62 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs113474791 | 4:17,851,508 | G/A | — | — |
| rs113591949 | 4:17,851,945 | A/G | — | — |
| rs16895888 | 4:17,853,921 | G/C | — | — |
| rs6842303 | 4:17,854,055 | T/C | — | — |
| rs79334166 | 4:17,859,466 | A/G | intron variant | — |
| rs113476736 | 4:17,864,274 | T/C | intron variant | — |
| rs74619517 | 4:17,865,561 | G/A | intron variant | — |
| rs185373991 | 4:17,865,864 | T/A | intron variant | — |
| rs73098804 | 4:17,865,865 | T/A | intron variant | — |
| rs57654001 | 4:17,866,866 | C/A | — | — |
| rs6817306 | 4:17,868,058 | T/C | intron variant | — |
| rs16895917 | 4:17,869,234 | T/C | intron variant | — |
| rs7671110 | 4:17,874,089 | C/T | intron variant | — |
| rs13131350 | 4:17,877,487 | A/T | — | — |
| rs148261312 | 4:17,885,731 | C/T | — | uncertain significance |
| rs985548800 | 4:17,885,844 | C/T | — | uncertain significance |
| rs1326311633 | 4:17,885,866 | C/G | — | uncertain significance |
| rs2475051081 | 4:17,885,892 | A/C | — | uncertain significance |
| rs2475051375 | 4:17,885,929 | G/A | — | uncertain significance |
| rs1030162874 | 4:17,885,930 | G/A | — | uncertain significance |
| rs766118294 | 4:17,886,188 | A/G | — | uncertain significance |
| rs1360462998 | 4:17,886,288 | C/G | — | uncertain significance |
| rs1288930412 | 4:17,886,334 | G/C | — | uncertain significance |
| rs2475055766 | 4:17,886,362 | T/G | — | uncertain significance |
| rs776619397 | 4:17,886,373 | C/T | — | uncertain significance |
| rs1728229076 | 4:17,887,695 | C/T | — | uncertain significance |
| rs1472852 | 4:17,910,236 | C/A | upstream gene variant | — |
| rs942459808 | 4:17,910,817 | T/G | — | uncertain significance |
| rs1321492437 | 4:17,910,828 | T/C | — | uncertain significance |
| rs759639568 | 4:17,910,845 | C/A | — | uncertain significance |
| rs1560325753 | 4:17,910,966 | G/A | — | uncertain significance |
| rs925098 | 4:17,919,811 | G/C | — | — |
| rs7692995 | 4:17,936,634 | T/C | intron variant | — |
| rs77998009 | 4:17,936,794 | G/A | intron variant | — |
| rs16896068 | 4:17,944,840 | G/A | intron variant | — |
| rs2724475 | 4:17,946,432 | T/A | — | — |
| rs71603393 | 4:17,950,968 | G/A | intron variant | — |
| rs6845078 | 4:17,952,208 | C/A | — | — |
| rs7686082 | 4:17,957,576 | C/T | intron variant | — |
| rs7673321 | 4:17,957,688 | T/A | intron variant | — |
| rs151054620 | 4:17,963,534 | C/T | — | uncertain significance |
| rs2475699314 | 4:17,964,631 | T/G | — | uncertain significance |
| rs34588175 | 4:17,967,114 | G/A | intron variant | — |
| rs34025766 | 4:17,968,811 | T/C | — | — |
| rs2724485 | 4:17,969,698 | T/C | intron variant | — |
| rs192246265 | 4:17,971,214 | T/G | intron variant | — |
| rs13144767 | 4:17,974,219 | A/G | intron variant | — |
| rs1280074118 | 4:17,974,470 | G/C | — | uncertain significance |
| rs724577 | 4:17,993,410 | A/G | — | — |
| rs6824748 | 4:17,997,066 | G/A | intron variant | — |
| rs16896239 | 4:18,004,755 | A/G | intron variant | — |
| rs6842114 | 4:18,008,199 | A/T | — | — |
| rs2610990 | 4:18,008,232 | A/G | intron variant | — |
| rs71603396 | 4:18,012,035 | G/A | intron variant | — |
| rs16896276 | 4:18,015,156 | T/A | intron variant | — |
| rs6830062 | 4:18,017,730 | T/C | intron variant | — |
| rs2610989 | 4:18,022,834 | T/C | regulatory region variant | — |
| rs888541058 | 4:18,023,306 | C/G | — | uncertain significance |
| rs1055803413 | 4:18,023,334 | G/A | — | uncertain significance |
| rs777722059 | 4:18,023,337 | G/A | — | uncertain significance |
| rs1725656705 | 4:18,023,371 | C/T | — | uncertain significance |
| rs2125654 | 4:18,025,368 | T/A | upstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.