VSIG10
V-set and immunoglobulin domain containing 10
Summary
Predicted to enable cell adhesion molecule binding activity. Predicted to be involved in cell-cell adhesion and synapse assembly. Predicted to be located in membrane. Predicted to be active in cell-cell junction and plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants41 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs548649623 | 12:118,503,342 | C/T | — | — |
| rs185858778 | 12:118,504,457 | T/C | — | uncertain significance |
| rs576551409 | 12:118,504,473 | T/C | — | uncertain significance |
| rs61943489 | 12:118,505,026 | G/T | upstream gene variant | — |
| rs984190468 | 12:118,506,212 | G/C | — | uncertain significance |
| rs374897815 | 12:118,506,245 | T/C | — | uncertain significance |
| rs372240626 | 12:118,506,256 | T/C | — | likely benign |
| rs2032347075 | 12:118,506,278 | G/T | — | uncertain significance |
| rs375116018 | 12:118,506,319 | G/A | — | uncertain significance |
| rs1208586145 | 12:118,509,187 | T/C | — | uncertain significance |
| rs2500758122 | 12:118,511,509 | A/T | — | uncertain significance |
| rs1442133084 | 12:118,511,579 | C/T | — | uncertain significance |
| rs1593498756 | 12:118,511,623 | C/A | — | uncertain significance |
| rs756484364 | 12:118,511,669 | C/T | — | uncertain significance |
| rs749544433 | 12:118,511,671 | G/C | — | uncertain significance |
| rs371765006 | 12:118,511,740 | G/A | — | uncertain significance |
| rs764371864 | 12:118,511,767 | T/C | — | uncertain significance |
| rs113691608 | 12:118,511,985 | G/A | intron variant | — |
| rs183562350 | 12:118,515,076 | C/T | intron variant | — |
| rs368571027 | 12:118,517,224 | A/T | — | uncertain significance |
| rs1221501943 | 12:118,517,282 | A/G | — | uncertain significance |
| rs372573416 | 12:118,517,310 | A/G | — | uncertain significance |
| rs774654305 | 12:118,517,339 | C/T | — | uncertain significance |
| rs924865818 | 12:118,517,350 | C/G | — | uncertain significance |
| rs938793654 | 12:118,517,351 | T/G | — | uncertain significance |
| rs2038499621 | 12:118,520,157 | A/T | — | uncertain significance |
| rs770204532 | 12:118,520,169 | C/T | — | uncertain significance |
| rs369510432 | 12:118,520,183 | T/C | — | uncertain significance |
| rs7957470 | 12:118,524,426 | A/G | intron variant | — |
| rs149410557 | 12:118,525,822 | G/A | intron variant | — |
| rs187513601 | 12:118,532,393 | T/G | intron variant | — |
| rs112561796 | 12:118,533,252 | C/T | intron variant | — |
| rs192950567 | 12:118,533,400 | A/G | — | uncertain significance |
| rs906864637 | 12:118,533,401 | T/C | — | uncertain significance |
| rs2033427525 | 12:118,533,448 | T/C | — | uncertain significance |
| rs142979297 | 12:118,533,464 | G/A | missense variant | — |
| rs377153797 | 12:118,533,517 | G/A | — | uncertain significance |
| rs372273973 | 12:118,533,526 | C/T | — | uncertain significance |
| rs2033432299 | 12:118,533,565 | C/T | — | uncertain significance |
| rs142883878 | 12:118,540,651 | T/C | intron variant | — |
| rs1001802159 | 12:118,541,455 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.