AACS
acetoacetyl-CoA synthetase
Summary
Predicted to enable acetoacetate-CoA ligase activity. Predicted to be involved in positive regulation of insulin secretion. Predicted to be located in cytosol. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants55 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1955670847 | 12:125,550,245 | G/A | — | uncertain significance |
| rs771455028 | 12:125,558,478 | G/A | — | uncertain significance |
| rs777018979 | 12:125,558,486 | G/T | — | uncertain significance |
| rs200646490 | 12:125,561,050 | C/T | — | uncertain significance |
| rs751807542 | 12:125,561,112 | C/T | — | uncertain significance |
| rs77474358 | 12:125,561,118 | C/T | — | uncertain significance |
| rs55999005 | 12:125,571,879 | C/T | intron variant | — |
| rs751926711 | 12:125,575,986 | A/G | — | uncertain significance |
| rs370916743 | 12:125,575,988 | T/A | — | uncertain significance |
| rs1384968719 | 12:125,576,004 | G/A | — | uncertain significance |
| rs762182856 | 12:125,576,056 | A/G | — | uncertain significance |
| rs915985549 | 12:125,587,228 | G/A | — | uncertain significance |
| rs755979712 | 12:125,587,298 | A/G | — | uncertain significance |
| rs2485607204 | 12:125,587,313 | T/C | — | uncertain significance |
| rs150718667 | 12:125,587,566 | G/T | — | uncertain significance |
| rs374355858 | 12:125,587,593 | A/G | — | uncertain significance |
| rs139116253 | 12:125,591,695 | G/A | — | uncertain significance |
| rs140471021 | 12:125,591,727 | C/T | — | benign |
| rs1049043798 | 12:125,591,728 | G/A | — | uncertain significance |
| rs140472203 | 12:125,591,734 | C/G | — | uncertain significance |
| rs775168357 | 12:125,591,763 | G/A | — | uncertain significance |
| rs2547247464 | 12:125,591,804 | A/T | — | uncertain significance |
| rs55657684 | 12:125,593,222 | A/T | intron variant | — |
| rs143681355 | 12:125,599,062 | G/A | — | uncertain significance |
| rs748407852 | 12:125,603,218 | C/A | — | uncertain significance |
| rs2547259955 | 12:125,603,229 | A/G | — | uncertain significance |
| rs757104418 | 12:125,603,257 | G/A | — | uncertain significance |
| rs142101780 | 12:125,603,275 | C/T | — | uncertain significance |
| rs772397111 | 12:125,603,276 | G/A | — | likely benign |
| rs373491989 | 12:125,603,281 | A/G | — | uncertain significance |
| rs181059565 | 12:125,609,467 | G/C | — | uncertain significance |
| rs769532481 | 12:125,609,478 | C/T | — | uncertain significance |
| rs151296809 | 12:125,609,551 | C/T | — | benign |
| rs548348280 | 12:125,612,743 | A/T | — | uncertain significance |
| rs199853330 | 12:125,612,762 | T/C | — | likely benign |
| rs573261809 | 12:125,612,799 | G/A | — | uncertain significance |
| rs763404617 | 12:125,612,814 | G/A | — | uncertain significance |
| rs768882103 | 12:125,613,904 | G/A | — | uncertain significance |
| rs762994345 | 12:125,613,947 | A/G | — | uncertain significance |
| rs766563338 | 12:125,618,566 | G/A | — | uncertain significance |
| rs371762205 | 12:125,618,614 | C/T | — | uncertain significance |
| rs145059717 | 12:125,619,360 | A/G | — | uncertain significance |
| rs143787385 | 12:125,619,382 | G/A | — | benign |
| rs2547275159 | 12:125,619,392 | A/T | — | uncertain significance |
| rs1349431927 | 12:125,619,395 | A/G | — | uncertain significance |
| rs77320648 | 12:125,621,219 | G/C | — | benign |
| rs748160942 | 12:125,621,249 | C/G | — | uncertain significance |
| rs746208598 | 12:125,621,352 | G/A | — | uncertain significance |
| rs773846020 | 12:125,621,358 | G/A | — | uncertain significance |
| rs200840579 | 12:125,621,418 | C/G | — | benign |
| rs749290306 | 12:125,626,665 | G/C | — | uncertain significance |
| rs761519431 | 12:125,626,671 | G/A | — | uncertain significance |
| rs765733198 | 12:125,626,698 | G/A | — | uncertain significance |
| rs768647856 | 12:125,626,725 | C/T | — | uncertain significance |
| rs188581486 | 12:125,626,746 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.