STARD10
StAR related lipid transfer domain containing 10
Summary
Predicted to enable lipid binding activity. Predicted to be involved in lipid transport. Predicted to act upstream of or within bile acid secretion and positive regulation of peroxisome proliferator activated receptor signaling pathway. Located in cytosol. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants25 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1858619471 | 11:72,465,946 | G/T | — | uncertain significance |
| rs374848566 | 11:72,465,960 | G/C | — | uncertain significance |
| rs202089909 | 11:72,465,974 | C/T | — | uncertain significance |
| rs73543261 | 11:72,466,017 | C/T | — | benign |
| rs766215581 | 11:72,466,030 | A/G | — | uncertain significance |
| rs764367371 | 11:72,466,060 | G/A | — | uncertain significance |
| rs750882418 | 11:72,466,079 | G/C | — | uncertain significance |
| rs368925280 | 11:72,466,102 | G/A | — | uncertain significance |
| rs1414929124 | 11:72,466,177 | T/A | — | uncertain significance |
| rs754719737 | 11:72,466,786 | T/G | — | uncertain significance |
| rs1858663557 | 11:72,468,847 | C/T | — | uncertain significance |
| rs1170316626 | 11:72,468,917 | G/A | — | uncertain significance |
| rs761639628 | 11:72,469,633 | C/T | — | uncertain significance |
| rs199726598 | 11:72,469,634 | G/A | — | uncertain significance |
| rs1446101248 | 11:72,470,302 | T/C | — | uncertain significance |
| rs898231686 | 11:72,470,423 | G/A | — | uncertain significance |
| rs116714277 | 11:72,473,447 | C/T | upstream gene variant | — |
| rs543505715 | 11:72,481,273 | A/T | — | — |
| rs1411430576 | 11:72,492,113 | C/A | — | uncertain significance |
| rs1858988168 | 11:72,492,121 | C/G | — | uncertain significance |
| rs771499208 | 11:72,492,169 | C/T | — | uncertain significance |
| rs775994344 | 11:72,492,175 | C/A | — | uncertain significance |
| rs2497223966 | 11:72,492,205 | T/C | — | uncertain significance |
| rs72964900 | 11:72,500,924 | C/T | regulatory region variant | — |
| rs519790 | 11:72,504,141 | C/G | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.