ATF7IP2
activating transcription factor 7 interacting protein 2
Summary
Predicted to enable transcription coregulator activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be part of transcription regulator complex. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants46 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs746102771 | 16:10,524,487 | C/A | — | uncertain significance |
| rs1431429824 | 16:10,524,556 | G/A | — | uncertain significance |
| rs542176148 | 16:10,524,590 | T/C | — | uncertain significance |
| rs149126039 | 16:10,524,608 | G/A | — | likely benign |
| rs1481652959 | 16:10,524,649 | A/G | — | uncertain significance |
| rs532117193 | 16:10,524,653 | C/G | — | likely benign |
| rs75627261 | 16:10,524,659 | C/T | — | uncertain significance |
| rs745848643 | 16:10,524,698 | C/T | — | uncertain significance |
| rs139175781 | 16:10,524,727 | A/G | — | likely benign |
| rs2506039400 | 16:10,524,815 | T/A | — | uncertain significance |
| rs141625467 | 16:10,524,821 | C/T | — | uncertain significance |
| rs774843896 | 16:10,524,877 | G/T | — | uncertain significance |
| rs766374861 | 16:10,524,928 | G/A | — | likely benign |
| rs2506039926 | 16:10,524,947 | A/G | — | uncertain significance |
| rs150784930 | 16:10,524,949 | C/T | — | uncertain significance |
| rs2506040273 | 16:10,525,037 | G/A | — | likely benign |
| rs1479558889 | 16:10,525,107 | T/A | — | uncertain significance |
| rs143268531 | 16:10,525,144 | G/C | — | uncertain significance |
| rs2048244725 | 16:10,525,196 | C/T | — | likely benign |
| rs775476351 | 16:10,525,238 | G/A | — | uncertain significance |
| rs148549701 | 16:10,525,258 | A/G | — | uncertain significance |
| rs372156472 | 16:10,527,436 | T/A | — | uncertain significance |
| rs190799715 | 16:10,527,490 | C/T | — | uncertain significance |
| rs2506060860 | 16:10,532,047 | G/T | — | uncertain significance |
| rs147875566 | 16:10,532,076 | T/C | — | uncertain significance |
| rs1490139355 | 16:10,532,078 | G/A | — | uncertain significance |
| rs374687929 | 16:10,532,086 | A/C | — | uncertain significance |
| rs749835754 | 16:10,534,222 | C/T | — | uncertain significance |
| rs377556995 | 16:10,534,256 | A/C | — | likely benign |
| rs573460456 | 16:10,534,294 | T/C | — | uncertain significance |
| rs1247870837 | 16:10,551,243 | G/C | — | uncertain significance |
| rs767001897 | 16:10,551,304 | A/C | — | uncertain significance |
| rs143609619 | 16:10,551,348 | T/G | — | uncertain significance |
| rs200149128 | 16:10,551,434 | T/C | intron variant | — |
| rs13335336 | 16:10,559,263 | A/G | intron variant | — |
| rs954097702 | 16:10,566,010 | T/A | — | uncertain significance |
| rs376890755 | 16:10,566,037 | A/G | — | uncertain significance |
| rs761792550 | 16:10,567,360 | A/G | — | uncertain significance |
| rs141649358 | 16:10,567,802 | C/G | — | uncertain significance |
| rs2506230239 | 16:10,574,787 | A/G | — | uncertain significance |
| rs762493285 | 16:10,574,790 | A/G | — | uncertain significance |
| rs756493244 | 16:10,574,804 | G/T | — | uncertain significance |
| rs774294368 | 16:10,575,724 | T/C | — | uncertain significance |
| rs188912843 | 16:10,575,810 | C/T | — | uncertain significance |
| rs1177993861 | 16:10,575,856 | A/G | — | uncertain significance |
| rs763494002 | 16:10,575,869 | G/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.