GATAD2A
GATA zinc finger domain containing 2A
Summary
Enables protein-macromolecule adaptor activity. Involved in chromatin remodeling and negative regulation of DNA-templated transcription. Located in nucleoplasm. Part of NuRD complex. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants79 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs10408875 | 19:19,503,573 | T/A | — | — |
| rs17288409 | 19:19,504,167 | T/C | intron variant | — |
| rs8111093 | 19:19,505,548 | C/G | — | — |
| rs111901094 | 19:19,513,570 | G/A | — | — |
| rs2916068 | 19:19,516,433 | A/G | regulatory region variant | — |
| rs142456630 | 19:19,520,276 | G/A | — | — |
| rs118056794 | 19:19,520,494 | C/T | intron variant | — |
| rs569528102 | 19:19,525,736 | A/T | — | — |
| rs1469713 | 19:19,528,806 | A/G | regulatory region variant | — |
| rs28478453 | 19:19,531,175 | C/G | intron variant | — |
| rs11669516 | 19:19,532,682 | G/T | — | — |
| rs4808199 | 19:19,545,099 | G/T | — | — |
| rs4808955 | 19:19,552,413 | T/C | intron variant | — |
| rs773676090 | 19:19,576,174 | G/A | — | uncertain significance |
| rs369745941 | 19:19,576,195 | C/T | — | uncertain significance |
| rs752197724 | 19:19,576,321 | C/T | — | uncertain significance |
| rs202247345 | 19:19,576,392 | G/A | — | uncertain significance |
| rs759128095 | 19:19,576,410 | C/T | — | uncertain significance |
| rs765001826 | 19:19,576,411 | G/A | — | uncertain significance |
| rs73002956 | 19:19,578,743 | A/G | intron variant | — |
| rs4808962 | 19:19,579,557 | A/G | intron variant | — |
| rs113070129 | 19:19,580,964 | G/A | — | — |
| rs117482399 | 19:19,581,290 | C/T | intron variant | — |
| rs73002960 | 19:19,582,992 | C/T | intron variant | — |
| rs116991940 | 19:19,589,253 | A/G | intron variant | — |
| rs145462963 | 19:19,595,378 | C/T | intron variant | — |
| rs189452885 | 19:19,596,133 | G/A | regulatory region variant | — |
| rs2315610 | 19:19,597,240 | T/C | intron variant | — |
| rs117204956 | 19:19,602,936 | C/T | intron variant | — |
| rs545460363 | 19:19,603,115 | T/C | — | likely benign |
| rs200305535 | 19:19,603,128 | G/A | — | uncertain significance |
| rs201367846 | 19:19,603,171 | A/G | — | uncertain significance |
| rs2513588500 | 19:19,603,192 | G/A | — | uncertain significance |
| rs1568333169 | 19:19,603,396 | A/T | — | uncertain significance |
| rs2513594785 | 19:19,603,415 | G/T | — | uncertain significance |
| rs779971463 | 19:19,603,489 | A/G | — | uncertain significance |
| rs748592461 | 19:19,605,137 | C/G | — | uncertain significance |
| rs761641047 | 19:19,605,175 | G/A | — | uncertain significance |
| rs570408424 | 19:19,606,203 | C/T | — | — |
| rs2082421 | 19:19,606,264 | C/T | intron variant | — |
| rs1000737028 | 19:19,606,564 | C/T | — | uncertain significance |
| rs2513650811 | 19:19,606,611 | C/T | — | uncertain significance |
| rs745531722 | 19:19,606,660 | A/C | — | uncertain significance |
| rs577666541 | 19:19,606,871 | G/A | — | likely benign |
| rs1238369613 | 19:19,607,014 | G/A | — | uncertain significance |
| rs367981840 | 19:19,607,018 | A/G | — | uncertain significance |
| rs1187109379 | 19:19,609,280 | C/T | — | uncertain significance |
| rs149886344 | 19:19,609,313 | C/T | — | uncertain significance |
| rs1008975400 | 19:19,609,358 | G/A | — | uncertain significance |
| rs377723110 | 19:19,609,384 | C/T | — | uncertain significance |
| rs2513697772 | 19:19,609,400 | A/C | — | uncertain significance |
| rs371284522 | 19:19,609,436 | C/T | — | uncertain significance |
| rs1413878395 | 19:19,609,465 | G/A | — | uncertain significance |
| rs1302914328 | 19:19,609,480 | A/C | — | uncertain significance |
| rs200919274 | 19:19,609,529 | A/C | — | uncertain significance |
| rs201876986 | 19:19,611,930 | G/T | — | uncertain significance |
| rs772922486 | 19:19,611,941 | G/A | — | uncertain significance |
| rs2148488668 | 19:19,611,984 | G/A | — | uncertain significance |
| rs2513751262 | 19:19,612,011 | G/A | — | uncertain significance |
| rs541934878 | 19:19,612,055 | A/G | — | uncertain significance |
| rs112281927 | 19:19,612,213 | C/T | — | likely benign |
| rs747431890 | 19:19,612,791 | G/A | — | uncertain significance |
| rs763124030 | 19:19,612,823 | C/T | — | uncertain significance |
| rs775585903 | 19:19,612,832 | A/C | — | uncertain significance |
| rs759389249 | 19:19,613,158 | C/T | — | uncertain significance |
| rs780260876 | 19:19,613,165 | C/T | — | uncertain significance |
| rs549651871 | 19:19,613,174 | C/T | — | uncertain significance |
| rs769597782 | 19:19,613,204 | C/T | — | uncertain significance |
| rs2060596760 | 19:19,613,237 | C/T | — | uncertain significance |
| rs2060597268 | 19:19,613,246 | T/C | — | uncertain significance |
| rs755382122 | 19:19,613,257 | G/A | — | uncertain significance |
| rs761325321 | 19:19,613,309 | A/G | — | uncertain significance |
| rs201273478 | 19:19,616,165 | C/G | — | uncertain significance |
| rs759053983 | 19:19,616,222 | G/A | — | uncertain significance |
| rs201591863 | 19:19,616,240 | T/C | — | uncertain significance |
| rs200707525 | 19:19,616,251 | C/T | — | uncertain significance |
| rs2060826441 | 19:19,616,264 | A/G | — | uncertain significance |
| rs147166404 | 19:19,618,645 | A/G | downstream gene variant | — |
| rs144176312 | 19:19,618,713 | C/T | downstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.