SDAD1
SDA1 domain containing 1
Summary
Predicted to be involved in ribosomal large subunit biogenesis and ribosomal large subunit export from nucleus. Predicted to act upstream of or within cellular response to leukemia inhibitory factor. Located in nucleolus and nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants47 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1355243904 | 4:76,871,911 | T/C | — | uncertain significance |
| rs138382679 | 4:76,871,949 | A/C | — | uncertain significance |
| rs759681675 | 4:76,877,145 | A/T | — | uncertain significance |
| rs139040292 | 4:76,877,162 | C/T | — | uncertain significance |
| rs149346502 | 4:76,877,183 | A/G | — | uncertain significance |
| rs771713404 | 4:76,877,210 | T/C | — | uncertain significance |
| rs769871264 | 4:76,877,225 | G/A | — | uncertain significance |
| rs752690471 | 4:76,878,491 | A/C | — | uncertain significance |
| rs114721568 | 4:76,878,531 | G/A | — | uncertain significance |
| rs372072498 | 4:76,878,723 | C/T | — | uncertain significance |
| rs2242472 | 4:76,878,727 | G/C | — | benign |
| rs372514480 | 4:76,878,807 | T/C | — | likely benign |
| rs114534142 | 4:76,878,836 | A/G | — | likely benign |
| rs768365902 | 4:76,878,843 | T/C | — | uncertain significance |
| rs773128775 | 4:76,881,276 | T/G | — | uncertain significance |
| rs2476380263 | 4:76,881,314 | C/G | — | uncertain significance |
| rs769879168 | 4:76,882,228 | G/T | — | uncertain significance |
| rs2476385483 | 4:76,882,414 | G/C | — | uncertain significance |
| rs754051760 | 4:76,882,451 | T/C | — | uncertain significance |
| rs55876513 | 4:76,883,698 | T/G | intron variant | — |
| rs6836404 | 4:76,883,715 | C/T | intron variant | — |
| rs746216898 | 4:76,885,340 | C/T | — | uncertain significance |
| rs570479713 | 4:76,888,474 | T/C | — | uncertain significance |
| rs184208240 | 4:76,888,497 | G/T | — | benign |
| rs2273 | 4:76,889,388 | C/T | intron variant | — |
| rs766891427 | 4:76,890,472 | A/C | — | uncertain significance |
| rs76310548 | 4:76,890,566 | G/A | intron variant | — |
| rs192289747 | 4:76,891,102 | C/T | intron variant | — |
| rs372493192 | 4:76,891,515 | T/C | — | uncertain significance |
| rs774926966 | 4:76,892,569 | T/C | — | uncertain significance |
| rs760103693 | 4:76,894,482 | G/C | — | uncertain significance |
| rs755061563 | 4:76,894,532 | C/A | — | uncertain significance |
| rs1578135428 | 4:76,894,541 | A/G | — | likely benign |
| rs373552511 | 4:76,895,266 | T/C | — | uncertain significance |
| rs1170740960 | 4:76,897,105 | G/T | — | uncertain significance |
| rs1405184007 | 4:76,897,106 | C/T | — | uncertain significance |
| rs2476442528 | 4:76,897,118 | T/G | — | uncertain significance |
| rs746467341 | 4:76,898,818 | T/C | — | uncertain significance |
| rs148278023 | 4:76,898,867 | T/C | — | uncertain significance |
| rs192716315 | 4:76,899,176 | T/C | upstream gene variant | — |
| rs2476465722 | 4:76,902,618 | A/C | — | uncertain significance |
| rs1730555372 | 4:76,903,175 | T/C | — | uncertain significance |
| rs117413297 | 4:76,903,185 | T/C | — | benign |
| rs72653605 | 4:76,910,225 | C/T | intron variant | — |
| rs72653606 | 4:76,910,761 | C/T | intron variant | — |
| rs1205378322 | 4:76,911,954 | G/A | — | uncertain significance |
| rs542154908 | 4:76,911,974 | G/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.