ITLN2
intelectin 2
Summary
Predicted to enable oligosaccharide binding activity. Predicted to be located in extracellular region. Predicted to be active in extracellular space. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants37 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs764392071 | 1:160,914,946 | A/G | — | uncertain significance |
| rs750788583 | 1:160,914,971 | G/A | — | uncertain significance |
| rs2525975085 | 1:160,915,016 | A/G | — | uncertain significance |
| rs149928906 | 1:160,915,019 | C/T | missense variant | — |
| rs1354978381 | 1:160,915,039 | C/T | — | uncertain significance |
| rs760111872 | 1:160,915,040 | G/A | — | likely benign |
| rs763748248 | 1:160,915,042 | G/A | — | uncertain significance |
| rs2525982619 | 1:160,917,732 | C/G | — | uncertain significance |
| rs373894051 | 1:160,917,774 | C/G | — | uncertain significance |
| rs12059277 | 1:160,919,628 | G/C | coding sequence variant | — |
| rs201391588 | 1:160,919,847 | G/A | — | uncertain significance |
| rs12094026 | 1:160,920,372 | G/A | — | benign |
| rs1409626034 | 1:160,920,389 | G/C | — | uncertain significance |
| rs143503379 | 1:160,920,427 | A/T | — | uncertain significance |
| rs12090411 | 1:160,920,431 | T/C | — | benign |
| rs754202122 | 1:160,920,438 | G/A | — | uncertain significance |
| rs745954582 | 1:160,920,464 | C/T | — | uncertain significance |
| rs779964792 | 1:160,920,483 | T/C | — | uncertain significance |
| rs201788372 | 1:160,920,838 | A/G | — | uncertain significance |
| rs147123034 | 1:160,920,846 | C/T | — | uncertain significance |
| rs137860437 | 1:160,920,855 | G/A | — | uncertain significance |
| rs141731306 | 1:160,920,865 | A/G | — | uncertain significance |
| rs61469377 | 1:160,920,902 | C/T | — | benign |
| rs2525993093 | 1:160,920,909 | T/C | — | uncertain significance |
| rs371200791 | 1:160,920,925 | C/T | — | uncertain significance |
| rs200061193 | 1:160,920,943 | G/T | — | uncertain significance |
| rs777804097 | 1:160,920,971 | G/C | — | uncertain significance |
| rs777412143 | 1:160,920,985 | C/T | — | uncertain significance |
| rs983275695 | 1:160,921,037 | C/A | — | uncertain significance |
| rs375483594 | 1:160,921,045 | C/T | — | likely benign |
| rs566398966 | 1:160,921,063 | G/A | — | likely benign |
| rs139210766 | 1:160,921,663 | C/A | regulatory region variant | — |
| rs550649438 | 1:160,922,428 | G/A | — | likely benign |
| rs373717915 | 1:160,922,463 | G/C | — | uncertain significance |
| rs148724799 | 1:160,922,481 | G/T | — | uncertain significance |
| rs189578621 | 1:160,924,612 | A/C | regulatory region variant | — |
| rs35112454 | 1:160,926,292 | T/C | upstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.