RETSAT
retinol saturase
Summary
Predicted to enable all-trans-retinol 13,14-reductase activity. Predicted to be involved in retinol metabolic process. Located in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants55 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs139022129 | 2:85,569,884 | G/T | upstream gene variant | — |
| rs761151422 | 2:85,570,381 | T/G | — | uncertain significance |
| rs753331463 | 2:85,570,385 | C/T | — | uncertain significance |
| rs71337786 | 2:85,570,388 | G/A | — | uncertain significance |
| rs71337784 | 2:85,570,430 | G/A | — | uncertain significance |
| rs1198176836 | 2:85,570,478 | C/G | — | uncertain significance |
| rs71337782 | 2:85,570,498 | T/C | — | uncertain significance |
| rs748224503 | 2:85,570,499 | C/A | — | uncertain significance |
| rs13384912 | 2:85,570,780 | G/T | — | uncertain significance |
| rs201163400 | 2:85,570,797 | C/T | — | uncertain significance |
| rs1683131247 | 2:85,570,822 | G/A | — | uncertain significance |
| rs371024263 | 2:85,570,827 | C/T | — | uncertain significance |
| rs754135784 | 2:85,570,893 | A/G | — | uncertain significance |
| rs2528642524 | 2:85,571,165 | G/A | — | uncertain significance |
| rs147993013 | 2:85,571,210 | C/T | — | uncertain significance |
| rs2528642932 | 2:85,571,241 | C/G | — | uncertain significance |
| rs771406290 | 2:85,571,366 | G/T | — | uncertain significance |
| rs762663446 | 2:85,571,385 | G/A | — | uncertain significance |
| rs1342276586 | 2:85,571,404 | A/G | — | uncertain significance |
| rs73945707 | 2:85,571,432 | C/T | — | benign |
| rs76973216 | 2:85,571,433 | G/A | — | benign |
| rs2528645420 | 2:85,571,786 | C/T | — | uncertain significance |
| rs142596961 | 2:85,571,789 | C/T | — | likely benign |
| rs374160271 | 2:85,571,825 | G/T | — | uncertain significance |
| rs559421827 | 2:85,571,834 | G/A | — | likely benign |
| rs138319569 | 2:85,573,114 | G/C | — | uncertain significance |
| rs371526032 | 2:85,573,155 | C/T | — | uncertain significance |
| rs769002387 | 2:85,573,178 | T/C | — | uncertain significance |
| rs376151430 | 2:85,573,212 | T/C | — | uncertain significance |
| rs115506643 | 2:85,573,726 | A/C | upstream gene variant | — |
| rs751471213 | 2:85,576,557 | G/C | — | uncertain significance |
| rs375130450 | 2:85,576,567 | C/T | — | uncertain significance |
| rs753129634 | 2:85,576,572 | C/T | — | uncertain significance |
| rs143321957 | 2:85,576,696 | G/C | — | uncertain significance |
| rs1416962965 | 2:85,576,701 | A/T | — | uncertain significance |
| rs141214963 | 2:85,577,182 | G/A | — | benign |
| rs982238600 | 2:85,577,273 | C/T | — | uncertain significance |
| rs150268408 | 2:85,577,285 | C/T | — | uncertain significance |
| rs749371023 | 2:85,577,295 | C/G | — | uncertain significance |
| rs2528661966 | 2:85,577,931 | A/T | — | uncertain significance |
| rs773940534 | 2:85,578,096 | A/T | — | uncertain significance |
| rs371286603 | 2:85,578,108 | A/G | — | uncertain significance |
| rs987565836 | 2:85,578,132 | A/G | — | uncertain significance |
| rs777682512 | 2:85,578,838 | T/C | — | uncertain significance |
| rs200407016 | 2:85,578,866 | G/T | — | uncertain significance |
| rs776079512 | 2:85,578,892 | G/A | — | uncertain significance |
| rs201423046 | 2:85,578,940 | A/G | — | uncertain significance |
| rs764080478 | 2:85,578,947 | C/T | — | uncertain significance |
| rs1209705960 | 2:85,578,958 | T/G | — | uncertain significance |
| rs147080219 | 2:85,578,987 | T/C | splice region variant | — |
| rs143067831 | 2:85,581,100 | A/C | regulatory region variant | — |
| rs201975804 | 2:85,581,461 | T/C | — | uncertain significance |
| rs200788156 | 2:85,581,465 | T/G | — | uncertain significance |
| rs1002406858 | 2:85,581,549 | T/C | — | uncertain significance |
| rs79796752 | 2:85,581,586 | G/A | — | benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.