ELOVL2
ELOVL fatty acid elongase 2
Summary
Enables fatty acid elongase activity. Involved in fatty acid elongation, polyunsaturated fatty acid and very long-chain fatty acid biosynthetic process. Located in endoplasmic reticulum. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants43 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs17606561 | 6:10,982,359 | G/A | downstream gene variant | — |
| rs3734398 | 6:10,982,973 | T/C | downstream gene variant | — |
| rs4532436 | 6:10,983,971 | C/A | — | — |
| rs372694220 | 6:10,984,034 | T/C | — | uncertain significance |
| rs751285613 | 6:10,984,097 | G/T | — | uncertain significance |
| rs367685105 | 6:10,984,121 | T/A | — | uncertain significance |
| rs9379992 | 6:10,984,330 | G/C | — | — |
| rs2093777 | 6:10,985,330 | T/C | — | — |
| rs146632589 | 6:10,986,228 | C/T | intron variant | — |
| rs9379996 | 6:10,986,812 | A/G | — | — |
| rs145581310 | 6:10,989,937 | T/C | — | uncertain significance |
| rs148461943 | 6:10,989,941 | C/T | — | uncertain significance |
| rs376331635 | 6:10,989,949 | T/C | — | uncertain significance |
| rs755894626 | 6:10,989,970 | G/A | — | uncertain significance |
| rs777096370 | 6:10,990,015 | C/G | — | uncertain significance |
| rs202019761 | 6:10,990,061 | C/T | — | uncertain significance |
| rs2281591 | 6:10,990,493 | A/C | — | — |
| rs1286690128 | 6:10,990,630 | T/C | — | uncertain significance |
| rs2236212 | 6:10,995,015 | G/C | intron variant | — |
| rs768479188 | 6:10,995,321 | T/C | — | uncertain significance |
| rs1405388259 | 6:10,995,336 | T/C | — | uncertain significance |
| rs867506828 | 6:10,995,339 | G/A | — | uncertain significance |
| rs996804777 | 6:10,995,342 | A/C | — | uncertain significance |
| rs9295741 | 6:10,997,166 | C/G | — | — |
| rs61624919 | 6:10,997,823 | G/C | — | — |
| rs758207633 | 6:11,000,322 | G/A | — | uncertain significance |
| rs777593032 | 6:11,000,323 | G/C | — | uncertain significance |
| rs2295601 | 6:11,005,686 | G/A | synonymous variant | — |
| rs781681671 | 6:11,005,751 | G/A | — | uncertain significance |
| rs3798713 | 6:11,008,622 | G/C | regulatory region variant | — |
| rs9295752 | 6:11,010,800 | T/A | — | — |
| rs374592281 | 6:11,010,981 | C/T | — | uncertain significance |
| rs200475733 | 6:11,011,011 | T/C | — | uncertain significance |
| rs9380025 | 6:11,011,074 | T/A | — | — |
| rs953413 | 6:11,012,859 | G/A | regulatory region variant | — |
| rs3756963 | 6:11,022,154 | T/C | intron variant | — |
| rs60376022 | 6:11,027,949 | A/C | — | — |
| rs2208338 | 6:11,028,654 | G/A | intron variant | — |
| rs3798719 | 6:11,036,825 | C/T | intron variant | — |
| rs3798722 | 6:11,040,423 | A/T | — | — |
| rs9393903 | 6:11,042,909 | G/A | upstream gene variant | — |
| rs9468308 | 6:11,044,068 | T/A | — | — |
| rs115367234 | 6:11,044,658 | C/T | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.