OLFM3
olfactomedin 3
Summary
Predicted to be involved in signal transduction. Predicted to be located in Golgi apparatus; extracellular region; and synapse. Predicted to be part of AMPA glutamate receptor complex. Predicted to be active in extracellular space. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants26 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs772362722 | 1:102,269,801 | T/C | — | uncertain significance |
| rs1206190270 | 1:102,269,832 | T/C | — | uncertain significance |
| rs146272537 | 1:102,269,916 | A/G | — | uncertain significance |
| rs201625717 | 1:102,269,939 | T/C | — | uncertain significance |
| rs553939764 | 1:102,270,100 | A/T | — | uncertain significance |
| rs2524143998 | 1:102,270,405 | C/T | — | uncertain significance |
| rs1378547924 | 1:102,271,638 | G/T | — | uncertain significance |
| rs4908185 | 1:102,283,539 | C/T | intron variant | — |
| rs776719691 | 1:102,290,602 | C/T | — | uncertain significance |
| rs1654795039 | 1:102,290,636 | G/A | — | uncertain significance |
| rs2524225367 | 1:102,290,662 | A/G | — | uncertain significance |
| rs61806268 | 1:102,290,672 | G/C | — | uncertain significance |
| rs948356235 | 1:102,290,687 | C/G | — | uncertain significance |
| rs537938960 | 1:102,290,744 | T/C | — | uncertain significance |
| rs138105539 | 1:102,290,760 | G/A | — | likely benign |
| rs376340720 | 1:102,290,798 | A/C | — | uncertain significance |
| rs566629297 | 1:102,296,225 | T/C | — | uncertain significance |
| rs748816968 | 1:102,302,451 | C/T | — | uncertain significance |
| rs11555850 | 1:102,302,510 | G/A | — | likely benign |
| rs370091997 | 1:102,302,539 | C/T | — | uncertain significance |
| rs1446471685 | 1:102,302,580 | G/C | — | uncertain significance |
| rs17125616 | 1:102,329,484 | T/C | downstream gene variant | — |
| rs528643921 | 1:102,397,229 | T/C | — | — |
| rs1336790 | 1:102,413,968 | C/G | intron variant | — |
| rs551162240 | 1:102,462,353 | A/C | — | uncertain significance |
| rs569772451 | 1:102,462,362 | G/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.