ISLR
immunoglobulin superfamily containing leucine rich repeat
Summary
Predicted to be involved in cell adhesion. Located in extracellular exosome. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants36 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs137923011 | 15:74,467,244 | G/A | — | benign |
| rs201880413 | 15:74,467,302 | G/A | — | uncertain significance |
| rs991366708 | 15:74,467,320 | C/G | — | uncertain significance |
| rs79206759 | 15:74,467,328 | C/T | — | benign |
| rs148769100 | 15:74,467,329 | G/A | missense variant | — |
| rs2505723954 | 15:74,467,366 | G/A | — | uncertain significance |
| rs370512115 | 15:74,467,449 | A/T | — | uncertain significance |
| rs1446367705 | 15:74,467,504 | G/C | — | uncertain significance |
| rs2072778030 | 15:74,467,539 | G/T | — | uncertain significance |
| rs781227156 | 15:74,467,627 | G/T | — | uncertain significance |
| rs149796219 | 15:74,467,645 | G/A | — | uncertain significance |
| rs769818994 | 15:74,467,668 | C/A | — | uncertain significance |
| rs367850327 | 15:74,467,711 | C/T | — | uncertain significance |
| rs114338290 | 15:74,467,733 | C/T | — | benign |
| rs1171148538 | 15:74,467,758 | G/A | — | uncertain significance |
| rs370000092 | 15:74,467,764 | G/A | — | uncertain significance |
| rs1430421838 | 15:74,467,782 | G/A | — | uncertain significance |
| rs146746279 | 15:74,467,792 | C/T | — | uncertain significance |
| rs11854957 | 15:74,467,796 | C/T | synonymous variant | — |
| rs747377808 | 15:74,467,810 | A/G | — | uncertain significance |
| rs770282258 | 15:74,467,824 | G/A | — | likely benign |
| rs369708223 | 15:74,467,869 | C/G | — | uncertain significance |
| rs919871053 | 15:74,467,941 | C/T | — | uncertain significance |
| rs199556849 | 15:74,467,942 | G/A | — | uncertain significance |
| rs149394388 | 15:74,468,003 | C/G | — | uncertain significance |
| rs370331490 | 15:74,468,052 | G/A | — | uncertain significance |
| rs2505725811 | 15:74,468,076 | C/A | — | uncertain significance |
| rs117441233 | 15:74,468,107 | G/A | — | uncertain significance |
| rs985746281 | 15:74,468,121 | G/A | — | uncertain significance |
| rs1567172893 | 15:74,468,217 | G/A | — | uncertain significance |
| rs201525515 | 15:74,468,223 | G/A | — | uncertain significance |
| rs768314274 | 15:74,468,236 | C/T | — | uncertain significance |
| rs146727249 | 15:74,468,238 | C/A | — | uncertain significance |
| rs376163086 | 15:74,468,269 | G/A | — | uncertain significance |
| rs868026730 | 15:74,468,311 | C/T | — | uncertain significance |
| rs770211289 | 15:74,468,340 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.