VSIG2
V-set and immunoglobulin domain containing 2
Summary
Predicted to be involved in lipid metabolic process. Predicted to be located in plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants30 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2497057179 | 11:124,617,487 | G/T | — | uncertain significance |
| rs768943606 | 11:124,617,492 | T/C | — | uncertain significance |
| rs765999056 | 11:124,617,523 | T/C | — | likely benign |
| rs2075713 | 11:124,617,939 | A/C | regulatory region variant | — |
| rs201340528 | 11:124,618,307 | G/A | — | uncertain significance |
| rs183266468 | 11:124,618,358 | G/A | — | likely benign |
| rs765251797 | 11:124,618,415 | C/T | — | uncertain significance |
| rs2497059865 | 11:124,618,566 | G/T | — | uncertain significance |
| rs140254144 | 11:124,618,599 | C/T | — | uncertain significance |
| rs753939828 | 11:124,618,600 | G/A | — | uncertain significance |
| rs766884202 | 11:124,618,606 | T/C | — | uncertain significance |
| rs745761096 | 11:124,618,628 | G/C | — | uncertain significance |
| rs2497060144 | 11:124,618,638 | A/G | — | uncertain significance |
| rs11604175 | 11:124,619,407 | C/T | downstream gene variant | — |
| rs530449056 | 11:124,619,611 | C/G | — | uncertain significance |
| rs148389397 | 11:124,619,648 | C/T | — | likely benign |
| rs754244446 | 11:124,619,649 | G/A | — | uncertain significance |
| rs1263897434 | 11:124,619,678 | C/T | — | uncertain significance |
| rs761373419 | 11:124,619,759 | G/C | — | uncertain significance |
| rs879432533 | 11:124,620,624 | T/G | — | uncertain significance |
| rs2497065849 | 11:124,620,658 | G/T | — | uncertain significance |
| rs371645773 | 11:124,620,735 | A/T | — | uncertain significance |
| rs144644469 | 11:124,620,766 | G/A | — | uncertain significance |
| rs779348475 | 11:124,621,340 | T/G | — | uncertain significance |
| rs747958171 | 11:124,621,392 | G/A | — | uncertain significance |
| rs1325001709 | 11:124,621,428 | A/G | — | uncertain significance |
| rs370823064 | 11:124,621,996 | A/G | — | uncertain significance |
| rs770843983 | 11:124,622,003 | C/T | — | uncertain significance |
| rs113439662 | 11:124,622,023 | A/T | — | uncertain significance |
| rs12541 | 11:124,623,492 | T/C | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.