POU2AF1
POU class 2 homeobox associating factor 1
Summary
Enables transcription coactivator activity. Involved in positive regulation of transcription by RNA polymerase II. Part of RNA polymerase II transcription regulator complex. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants28 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1042752 | 11:111,223,111 | A/G | downstream gene variant | — |
| rs12417556 | 11:111,223,445 | G/A | downstream gene variant | — |
| rs140834337 | 11:111,225,020 | G/A | — | uncertain significance |
| rs764165808 | 11:111,225,034 | A/C | — | uncertain significance |
| rs2496628315 | 11:111,225,110 | A/G | — | uncertain significance |
| rs761279575 | 11:111,225,170 | G/A | — | uncertain significance |
| rs1860803795 | 11:111,225,210 | G/C | — | uncertain significance |
| rs1472937071 | 11:111,225,237 | G/T | — | uncertain significance |
| rs4387383 | 11:111,227,170 | T/C | — | benign |
| rs752535146 | 11:111,228,342 | G/T | — | uncertain significance |
| rs1591190546 | 11:111,228,343 | T/G | — | uncertain significance |
| rs147874251 | 11:111,228,370 | C/T | — | uncertain significance |
| rs2496639957 | 11:111,228,372 | G/A | — | uncertain significance |
| rs139875225 | 11:111,228,401 | A/G | — | likely benign |
| rs143769469 | 11:111,228,438 | G/A | — | benign |
| rs35664667 | 11:111,228,529 | T/C | — | likely benign |
| rs768764083 | 11:111,228,566 | G/A | — | likely benign |
| rs73005676 | 11:111,229,101 | T/C | — | — |
| rs12282082 | 11:111,229,470 | T/C | — | benign |
| rs116229465 | 11:111,229,531 | T/C | — | benign |
| rs35454698 | 11:111,229,546 | G/A | — | benign |
| rs1860949027 | 11:111,229,623 | G/A | — | uncertain significance |
| rs12419634 | 11:111,239,365 | G/C | intron variant | — |
| rs34880462 | 11:111,246,143 | G/T | — | — |
| rs4622303 | 11:111,248,514 | C/G | — | benign |
| rs4283016 | 11:111,248,640 | G/A | — | benign |
| rs11213863 | 11:111,249,785 | C/G | — | benign |
| rs10789825 | 11:111,249,819 | A/G | — | benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.