VSIG10L
V-set and immunoglobulin domain containing 10 like
Summary
Located in nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants62 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1985412626 | 19:51,837,054 | C/G | — | uncertain significance |
| rs1599831835 | 19:51,837,144 | G/A | — | likely benign |
| rs1187455444 | 19:51,837,532 | C/T | — | uncertain significance |
| rs753753190 | 19:51,837,543 | T/A | — | uncertain significance |
| rs111872099 | 19:51,837,565 | G/A | — | benign |
| rs139204023 | 19:51,839,921 | C/T | upstream gene variant | — |
| rs898235332 | 19:51,840,498 | G/A | — | uncertain significance |
| rs867947506 | 19:51,840,525 | C/T | — | uncertain significance |
| rs1008112869 | 19:51,840,533 | C/T | — | uncertain significance |
| rs1401695354 | 19:51,840,554 | C/T | — | uncertain significance |
| rs1340177192 | 19:51,840,747 | C/T | — | uncertain significance |
| rs2514129140 | 19:51,840,761 | T/C | — | uncertain significance |
| rs1293446524 | 19:51,841,263 | G/C | — | uncertain significance |
| rs865996246 | 19:51,841,289 | G/A | — | conflicting classifications of pathogenicity |
| rs57710066 | 19:51,841,312 | C/T | — | benign |
| rs2514130135 | 19:51,841,342 | C/G | — | uncertain significance |
| rs200590126 | 19:51,841,348 | C/T | missense variant | — |
| rs201452734 | 19:51,841,364 | G/A | missense variant | — |
| rs751537282 | 19:51,841,399 | A/G | — | uncertain significance |
| rs1002255545 | 19:51,841,430 | C/A | — | uncertain significance |
| rs532340677 | 19:51,841,437 | A/C | — | uncertain significance |
| rs200219374 | 19:51,841,459 | G/T | — | uncertain significance |
| rs1268420589 | 19:51,842,214 | G/A | — | uncertain significance |
| rs2514131789 | 19:51,842,276 | G/A | — | uncertain significance |
| rs2514131801 | 19:51,842,282 | C/A | — | uncertain significance |
| rs1568462808 | 19:51,842,292 | G/C | — | uncertain significance |
| rs192962117 | 19:51,842,357 | C/A | — | uncertain significance |
| rs981765664 | 19:51,842,381 | G/A | — | uncertain significance |
| rs1339945003 | 19:51,843,310 | G/C | — | uncertain significance |
| rs2514133593 | 19:51,843,398 | C/G | — | uncertain significance |
| rs2514133745 | 19:51,843,460 | C/T | — | uncertain significance |
| rs1011966855 | 19:51,843,469 | G/A | — | uncertain significance |
| rs887428690 | 19:51,843,485 | C/T | — | uncertain significance |
| rs1014781902 | 19:51,843,527 | C/G | — | uncertain significance |
| rs1483930925 | 19:51,843,553 | T/C | — | uncertain significance |
| rs148937058 | 19:51,843,677 | C/T | — | benign |
| rs757949932 | 19:51,843,729 | G/A | — | uncertain significance |
| rs555836839 | 19:51,843,737 | A/C | — | uncertain significance |
| rs778222475 | 19:51,843,788 | A/C | — | uncertain significance |
| rs2514134610 | 19:51,843,793 | G/T | — | uncertain significance |
| rs1312956757 | 19:51,843,825 | C/T | — | uncertain significance |
| rs1404532351 | 19:51,843,896 | C/G | — | uncertain significance |
| rs926044900 | 19:51,843,929 | C/A | — | uncertain significance |
| rs2514135011 | 19:51,843,951 | T/C | — | uncertain significance |
| rs1370961357 | 19:51,844,415 | C/A | — | uncertain significance |
| rs1379812689 | 19:51,844,454 | C/T | — | uncertain significance |
| rs760564636 | 19:51,844,469 | G/A | — | uncertain significance |
| rs189447976 | 19:51,844,688 | G/A | — | uncertain significance |
| rs758667475 | 19:51,844,722 | G/T | — | uncertain significance |
| rs1364149520 | 19:51,844,799 | A/C | — | uncertain significance |
| rs187051163 | 19:51,844,805 | T/A | — | uncertain significance |
| rs550590410 | 19:51,844,808 | G/A | — | uncertain significance |
| rs1206885627 | 19:51,844,821 | A/C | — | uncertain significance |
| rs1387717368 | 19:51,844,892 | G/T | — | uncertain significance |
| rs2514136803 | 19:51,844,898 | G/C | — | uncertain significance |
| rs2514136815 | 19:51,844,908 | G/A | — | uncertain significance |
| rs924521090 | 19:51,844,985 | G/A | — | likely benign |
| rs1380733855 | 19:51,845,013 | C/T | — | uncertain significance |
| rs141732375 | 19:51,845,070 | A/T | — | benign |
| rs1438844592 | 19:51,845,165 | T/A | — | uncertain significance |
| rs757056621 | 19:51,845,217 | G/C | — | uncertain significance |
| rs1359257261 | 19:51,845,373 | G/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.