ANXA1
annexin A1
Summary
This gene encodes a membrane-localized protein that binds phospholipids. This protein inhibits phospholipase A2 and has anti-inflammatory activity. Loss of function or expression of this gene has been detected in multiple tumors. [provided by RefSeq, Dec 2014]
Known Variants33 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs35304764 | 9:75,773,649 | G/T | — | benign |
| rs11557052 | 9:75,773,671 | A/T | — | uncertain significance |
| rs10114350 | 9:75,774,238 | T/C | — | benign |
| rs144842081 | 9:75,774,299 | G/A | — | uncertain significance |
| rs1269877580 | 9:75,775,175 | G/T | — | likely benign |
| rs753709791 | 9:75,775,186 | A/T | — | uncertain significance |
| rs2490390200 | 9:75,775,195 | T/G | — | uncertain significance |
| rs1329979405 | 9:75,775,216 | A/G | — | uncertain significance |
| rs550451804 | 9:75,775,287 | A/T | — | uncertain significance |
| rs368581314 | 9:75,775,299 | C/T | — | benign |
| rs543730068 | 9:75,775,728 | A/G | — | uncertain significance |
| rs62541553 | 9:75,777,421 | C/T | intron variant | — |
| rs368085989 | 9:75,777,728 | C/G | — | uncertain significance |
| rs754419431 | 9:75,777,737 | C/T | — | uncertain significance |
| rs778889698 | 9:75,778,416 | G/A | — | uncertain significance |
| rs115362505 | 9:75,778,451 | A/G | — | benign |
| rs201583819 | 9:75,780,027 | G/T | — | likely benign |
| rs149033255 | 9:75,780,055 | G/A | — | benign |
| rs2490397287 | 9:75,780,061 | G/T | — | uncertain significance |
| rs2490397294 | 9:75,780,062 | G/A | — | uncertain significance |
| rs960791340 | 9:75,780,066 | C/G | — | uncertain significance |
| rs369329871 | 9:75,780,076 | C/T | — | likely benign |
| rs144643143 | 9:75,780,087 | C/A | — | benign |
| rs2490397429 | 9:75,780,102 | G/A | — | uncertain significance |
| rs138602190 | 9:75,780,119 | C/T | — | uncertain significance |
| rs775791748 | 9:75,781,028 | C/A | — | uncertain significance |
| rs1470954682 | 9:75,782,419 | G/A | — | uncertain significance |
| rs150591447 | 9:75,782,445 | G/T | — | uncertain significance |
| rs181802457 | 9:75,782,481 | A/G | — | likely benign |
| rs779798345 | 9:75,783,972 | T/A | — | uncertain significance |
| rs746524290 | 9:75,783,975 | A/C | — | uncertain significance |
| rs1824282924 | 9:75,784,060 | A/T | — | uncertain significance |
| rs2811226 | 9:75,784,264 | G/A | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.