GABPB2
GA binding protein transcription factor subunit beta 2
Summary
Enables transcription cis-regulatory region binding activity. Acts upstream of or within positive regulation of transcription by RNA polymerase II. Located in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants28 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs587652578 | 1:151,043,526 | C/T | — | — |
| rs4970936 | 1:151,044,037 | C/T | regulatory region variant | — |
| rs11204771 | 1:151,054,180 | G/T | — | — |
| rs772956915 | 1:151,062,949 | G/A | — | uncertain significance |
| rs770534366 | 1:151,062,961 | G/T | — | uncertain significance |
| rs767459865 | 1:151,062,978 | A/G | — | uncertain significance |
| rs1678578640 | 1:151,062,993 | C/T | — | uncertain significance |
| rs760498129 | 1:151,063,014 | G/A | — | uncertain significance |
| rs763771799 | 1:151,063,024 | C/T | — | uncertain significance |
| rs748477841 | 1:151,065,699 | T/A | — | uncertain significance |
| rs143714520 | 1:151,065,732 | G/A | — | likely benign |
| rs2524707090 | 1:151,065,804 | A/G | — | uncertain significance |
| rs2524725318 | 1:151,070,329 | A/G | — | uncertain significance |
| rs757565806 | 1:151,070,338 | A/G | — | uncertain significance |
| rs2101519493 | 1:151,070,430 | G/A | — | uncertain significance |
| rs934742844 | 1:151,070,452 | C/G | — | uncertain significance |
| rs149260680 | 1:151,076,050 | C/T | — | uncertain significance |
| rs587689291 | 1:151,076,076 | A/G | — | uncertain significance |
| rs148044296 | 1:151,079,552 | C/T | — | uncertain significance |
| rs145125051 | 1:151,079,590 | G/A | — | uncertain significance |
| rs1433148865 | 1:151,079,617 | C/T | — | uncertain significance |
| rs766237084 | 1:151,079,627 | A/G | — | uncertain significance |
| rs140700719 | 1:151,079,654 | G/A | — | uncertain significance |
| rs376385809 | 1:151,089,987 | A/G | — | uncertain significance |
| rs1446450664 | 1:151,090,554 | A/C | — | uncertain significance |
| rs763705533 | 1:151,090,578 | A/G | — | likely benign |
| rs750051024 | 1:151,090,593 | C/T | — | uncertain significance |
| rs2524837924 | 1:151,090,728 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.