OLFML2A
olfactomedin like 2A
Summary
Predicted to enable extracellular matrix binding activity and identical protein binding activity. Predicted to be involved in signal transduction. Predicted to act upstream of or within extracellular matrix organization. Predicted to be located in extracellular matrix and extracellular region. Predicted to be active in extracellular space. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants75 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs980296301 | 9:127,539,569 | C/A | — | uncertain significance |
| rs753855958 | 9:127,549,258 | T/G | — | uncertain significance |
| rs549641804 | 9:127,549,306 | G/A | — | uncertain significance |
| rs779448921 | 9:127,549,317 | A/C | — | uncertain significance |
| rs372948738 | 9:127,549,324 | G/A | — | uncertain significance |
| rs371169223 | 9:127,549,371 | C/T | — | uncertain significance |
| rs2490571992 | 9:127,549,453 | T/C | — | uncertain significance |
| rs201760376 | 9:127,549,458 | C/T | — | uncertain significance |
| rs200109271 | 9:127,549,470 | G/A | — | uncertain significance |
| rs2490572083 | 9:127,549,472 | G/C | — | uncertain significance |
| rs200507889 | 9:127,549,495 | A/G | — | uncertain significance |
| rs1442435556 | 9:127,557,312 | A/C | — | uncertain significance |
| rs373492057 | 9:127,557,366 | G/A | — | uncertain significance |
| rs1384652053 | 9:127,561,571 | A/G | — | likely benign |
| rs780409580 | 9:127,561,586 | G/A | — | uncertain significance |
| rs533587628 | 9:127,561,615 | C/G | — | uncertain significance |
| rs79134766 | 9:127,561,723 | G/T | missense variant | — |
| rs961076024 | 9:127,563,888 | C/T | — | uncertain significance |
| rs200657468 | 9:127,563,889 | G/A | — | uncertain significance |
| rs116205949 | 9:127,563,930 | G/C | — | uncertain significance |
| rs564945864 | 9:127,566,374 | C/G | — | uncertain significance |
| rs548410915 | 9:127,566,412 | C/T | — | uncertain significance |
| rs1347996157 | 9:127,566,456 | G/A | — | uncertain significance |
| rs2490611451 | 9:127,566,459 | G/A | — | uncertain significance |
| rs775298341 | 9:127,566,478 | C/T | — | uncertain significance |
| rs753067335 | 9:127,566,514 | C/A | — | uncertain significance |
| rs145832280 | 9:127,566,525 | A/G | — | likely benign |
| rs746784403 | 9:127,566,534 | A/C | — | uncertain significance |
| rs2131274201 | 9:127,566,537 | A/C | — | uncertain significance |
| rs1293277730 | 9:127,566,540 | A/C | — | uncertain significance |
| rs904769007 | 9:127,566,543 | A/G | — | uncertain significance |
| rs776259571 | 9:127,566,544 | C/T | — | uncertain significance |
| rs565548539 | 9:127,566,546 | G/A | — | likely benign |
| rs768023390 | 9:127,566,552 | A/C | — | likely benign |
| rs776049632 | 9:127,566,555 | A/C | — | uncertain significance |
| rs138399306 | 9:127,566,582 | C/A | — | uncertain significance |
| rs1382546911 | 9:127,566,592 | C/T | — | uncertain significance |
| rs528086186 | 9:127,568,065 | T/G | — | — |
| rs373942886 | 9:127,570,068 | G/A | — | uncertain significance |
| rs1841928108 | 9:127,570,075 | G/C | — | uncertain significance |
| rs1338527443 | 9:127,570,077 | G/A | — | uncertain significance |
| rs777158838 | 9:127,570,080 | G/A | — | uncertain significance |
| rs148019218 | 9:127,570,089 | C/T | — | uncertain significance |
| rs745323595 | 9:127,570,113 | C/T | — | uncertain significance |
| rs200440505 | 9:127,570,134 | G/A | — | uncertain significance |
| rs763955338 | 9:127,570,137 | G/A | — | uncertain significance |
| rs547560612 | 9:127,570,141 | C/T | — | uncertain significance |
| rs1270357236 | 9:127,570,180 | A/G | — | uncertain significance |
| rs1240962841 | 9:127,570,195 | A/G | — | uncertain significance |
| rs778107421 | 9:127,570,240 | A/T | — | uncertain significance |
| rs144365777 | 9:127,572,113 | C/T | — | uncertain significance |
| rs150798539 | 9:127,572,128 | G/A | — | uncertain significance |
| rs756156410 | 9:127,572,138 | A/T | — | uncertain significance |
| rs1424855041 | 9:127,572,182 | A/G | — | uncertain significance |
| rs766685476 | 9:127,572,188 | A/G | — | uncertain significance |
| rs565853896 | 9:127,572,200 | G/A | — | uncertain significance |
| rs371035353 | 9:127,572,245 | G/A | — | uncertain significance |
| rs1403672596 | 9:127,572,272 | A/G | — | uncertain significance |
| rs149782630 | 9:127,572,282 | G/T | — | uncertain significance |
| rs368549348 | 9:127,572,305 | G/T | — | uncertain significance |
| rs140626253 | 9:127,572,311 | G/A | — | uncertain significance |
| rs754626358 | 9:127,572,317 | G/A | — | uncertain significance |
| rs777076931 | 9:127,572,341 | G/A | — | uncertain significance |
| rs776051451 | 9:127,572,350 | C/A | — | uncertain significance |
| rs755686037 | 9:127,572,401 | G/A | — | uncertain significance |
| rs748788898 | 9:127,572,410 | G/A | — | uncertain significance |
| rs759322338 | 9:127,572,437 | C/T | — | uncertain significance |
| rs1004147465 | 9:127,572,545 | C/G | — | uncertain significance |
| rs779101234 | 9:127,572,548 | A/C | — | uncertain significance |
| rs765852707 | 9:127,572,564 | G/A | — | likely benign |
| rs779002596 | 9:127,572,587 | G/A | — | uncertain significance |
| rs1841985551 | 9:127,572,591 | A/G | — | uncertain significance |
| rs373271578 | 9:127,572,593 | G/A | — | uncertain significance |
| rs748912745 | 9:127,572,682 | C/G | — | uncertain significance |
| rs770591877 | 9:127,572,683 | G/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.