OLFM2
olfactomedin 2
Summary
Involved in positive regulation of smooth muscle cell differentiation. Acts upstream of or within protein secretion. Located in cytoplasm; extracellular region; and nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants34 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs8111802 | 19:9,964,823 | A/G | — | benign |
| rs1419683310 | 19:9,964,880 | G/T | — | uncertain significance |
| rs11556088 | 19:9,964,946 | G/A | — | benign |
| rs1472323502 | 19:9,964,978 | T/C | — | uncertain significance |
| rs368014281 | 19:9,965,188 | C/G | — | uncertain significance |
| rs773856461 | 19:9,965,305 | C/T | — | uncertain significance |
| rs751696026 | 19:9,965,341 | G/A | — | uncertain significance |
| rs778414799 | 19:9,965,368 | C/T | — | uncertain significance |
| rs752885457 | 19:9,965,481 | C/T | — | uncertain significance |
| rs543038640 | 19:9,965,506 | G/A | — | uncertain significance |
| rs1296816270 | 19:9,965,530 | T/C | — | uncertain significance |
| rs8100089 | 19:9,965,545 | G/A | — | benign |
| rs16996141 | 19:9,965,692 | T/C | — | benign |
| rs34631855 | 19:9,967,429 | T/C | — | benign |
| rs1289831457 | 19:9,967,485 | G/A | — | uncertain significance |
| rs774239947 | 19:9,967,493 | G/A | — | uncertain significance |
| rs1207350566 | 19:9,967,551 | C/T | — | likely benign |
| rs749261299 | 19:9,967,572 | C/T | — | uncertain significance |
| rs376109829 | 19:9,968,118 | G/C | — | uncertain significance |
| rs11556087 | 19:9,968,139 | G/A | — | benign |
| rs201455202 | 19:9,968,429 | G/A | — | uncertain significance |
| rs2303100 | 19:9,968,434 | T/C | — | benign |
| rs1367342976 | 19:9,968,452 | A/G | — | uncertain significance |
| rs769224119 | 19:9,968,468 | C/T | — | likely benign |
| rs2513398467 | 19:9,971,332 | G/T | — | uncertain significance |
| rs377196769 | 19:9,971,346 | C/T | — | uncertain significance |
| rs756588056 | 19:9,971,347 | G/A | — | uncertain significance |
| rs2513398531 | 19:9,971,358 | T/C | — | uncertain significance |
| rs774935522 | 19:9,971,374 | T/C | — | uncertain significance |
| rs10415033 | 19:9,971,636 | C/T | — | benign |
| rs10413248 | 19:9,984,096 | T/G | — | — |
| rs1862471 | 19:10,000,322 | C/G | intron variant | — |
| rs2513455678 | 19:10,047,039 | A/T | — | uncertain significance |
| rs190031895 | 19:10,047,156 | C/A | — | benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.