HAGHL
hydroxyacylglutathione hydrolase like
Summary
Predicted to enable hydroxyacylglutathione hydrolase activity. Predicted to be involved in methylglyoxal catabolic process to D-lactate via S-lactoyl-glutathione. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants27 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1406812 | 16:777,121 | T/C | regulatory region variant | — |
| rs2544122531 | 16:777,531 | G/C | — | uncertain significance |
| rs138574766 | 16:777,533 | G/C | synonymous variant | — |
| rs755242305 | 16:777,567 | G/A | — | uncertain significance |
| rs759963866 | 16:777,596 | C/A | — | uncertain significance |
| rs748523464 | 16:778,117 | G/A | — | uncertain significance |
| rs1316226583 | 16:778,135 | C/G | — | likely benign |
| rs1406815 | 16:778,158 | C/T | synonymous variant | — |
| rs1301518035 | 16:778,181 | A/C | — | uncertain significance |
| rs947423137 | 16:778,325 | A/G | — | uncertain significance |
| rs756866510 | 16:778,330 | C/A | — | uncertain significance |
| rs1282636290 | 16:778,516 | C/G | — | uncertain significance |
| rs374833821 | 16:778,534 | C/G | — | uncertain significance |
| rs1313641707 | 16:778,804 | G/A | — | uncertain significance |
| rs777661176 | 16:778,809 | C/T | — | uncertain significance |
| rs773681350 | 16:778,834 | A/C | — | uncertain significance |
| rs755156372 | 16:778,869 | G/A | — | uncertain significance |
| rs369303595 | 16:779,027 | G/A | — | uncertain significance |
| rs1246988633 | 16:779,049 | T/C | — | uncertain significance |
| rs1420262296 | 16:779,057 | G/A | — | uncertain significance |
| rs1194601357 | 16:779,313 | G/A | — | uncertain significance |
| rs2544166682 | 16:779,325 | C/A | — | uncertain significance |
| rs1257737431 | 16:779,361 | G/A | — | uncertain significance |
| rs750025153 | 16:779,365 | G/C | — | uncertain significance |
| rs778813123 | 16:779,386 | C/T | — | uncertain significance |
| rs1027304689 | 16:779,434 | T/C | — | uncertain significance |
| rs1376042262 | 16:779,443 | C/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.