GASK1A
golgi associated kinase 1A
Summary
Located in intracellular membrane-bounded organelle. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants40 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs186228023 | 3:43,025,968 | T/G | intron variant | — |
| rs553601709 | 3:43,033,207 | T/C | — | — |
| rs184906538 | 3:43,037,354 | C/G | intron variant | — |
| rs3953390 | 3:43,055,847 | A/C | intron variant | — |
| rs557007733 | 3:43,073,771 | C/T | — | likely benign |
| rs368973802 | 3:43,073,772 | G/A | — | uncertain significance |
| rs1353342217 | 3:43,073,783 | C/T | — | uncertain significance |
| rs761424713 | 3:43,073,795 | C/T | — | uncertain significance |
| rs1025664846 | 3:43,073,834 | G/A | — | uncertain significance |
| rs138304813 | 3:43,073,835 | C/T | — | likely benign |
| rs571794011 | 3:43,073,873 | G/A | — | likely benign |
| rs904303617 | 3:43,073,936 | C/T | — | uncertain significance |
| rs1001225843 | 3:43,073,937 | G/A | — | uncertain significance |
| rs777185918 | 3:43,073,967 | G/A | — | uncertain significance |
| rs115672213 | 3:43,074,371 | G/C | — | benign |
| rs1378835483 | 3:43,074,450 | C/G | — | uncertain significance |
| rs2089586270 | 3:43,074,513 | C/G | — | uncertain significance |
| rs540079615 | 3:43,074,524 | G/T | — | uncertain significance |
| rs1214921895 | 3:43,074,557 | A/T | — | uncertain significance |
| rs779846844 | 3:43,074,559 | G/C | — | uncertain significance |
| rs752883117 | 3:43,074,722 | C/A | — | uncertain significance |
| rs746644564 | 3:43,074,804 | G/A | — | uncertain significance |
| rs376799926 | 3:43,074,810 | A/G | — | uncertain significance |
| rs778481022 | 3:43,074,825 | C/T | — | uncertain significance |
| rs2528834921 | 3:43,074,827 | T/C | — | uncertain significance |
| rs958646266 | 3:43,074,905 | G/A | — | uncertain significance |
| rs376613226 | 3:43,074,990 | C/T | — | likely benign |
| rs749233450 | 3:43,075,017 | G/A | — | uncertain significance |
| rs686464 | 3:43,085,649 | A/T | — | — |
| rs487463 | 3:43,085,726 | G/C | intron variant | — |
| rs62247127 | 3:43,086,564 | C/T | intron variant | — |
| rs1523123 | 3:43,091,017 | G/A | intron variant | — |
| rs17075122 | 3:43,094,678 | C/T | intron variant | — |
| rs765996836 | 3:43,095,019 | G/A | — | uncertain significance |
| rs747811986 | 3:43,095,032 | G/A | — | uncertain significance |
| rs1575453861 | 3:43,095,104 | A/G | — | uncertain significance |
| rs1175782993 | 3:43,096,975 | C/A | — | uncertain significance |
| rs375211654 | 3:43,097,684 | G/A | — | uncertain significance |
| rs577244724 | 3:43,097,696 | G/A | — | likely benign |
| rs866865751 | 3:43,097,768 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.