HMG20A
high mobility group 20A
Summary
Enables identical protein binding activity. Predicted to be involved in regulation of gene expression. Predicted to act upstream of or within negative regulation of neuron differentiation; negative regulation of protein sumoylation; and negative regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants36 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs62007299 | 15:77,711,719 | G/T | — | — |
| rs8024485 | 15:77,718,368 | C/G | — | — |
| rs17471252 | 15:77,738,682 | A/T | intron variant | — |
| rs1565756 | 15:77,741,640 | G/A | intron variant | — |
| rs7178572 | 15:77,747,190 | A/C | — | — |
| rs11633054 | 15:77,747,276 | A/T | — | — |
| rs61755713 | 15:77,750,749 | G/A | — | likely benign |
| rs61755712 | 15:77,750,775 | C/T | — | likely benign |
| rs372649225 | 15:77,750,781 | C/T | — | uncertain significance |
| rs747117781 | 15:77,750,803 | C/T | — | likely benign |
| rs112061352 | 15:77,756,608 | G/A | — | uncertain significance |
| rs538992863 | 15:77,756,668 | A/G | — | uncertain significance |
| rs1296081299 | 15:77,759,534 | G/A | — | uncertain significance |
| rs566884178 | 15:77,762,255 | C/T | — | — |
| rs1044909978 | 15:77,763,285 | C/T | — | uncertain significance |
| rs1356460765 | 15:77,763,339 | A/C | — | uncertain significance |
| rs1473677059 | 15:77,763,357 | C/T | — | uncertain significance |
| rs6495240 | 15:77,766,556 | T/G | — | — |
| rs12324627 | 15:77,767,539 | A/G | intron variant | — |
| rs373468221 | 15:77,769,919 | G/A | — | uncertain significance |
| rs2549226363 | 15:77,769,961 | A/G | — | uncertain significance |
| rs750449982 | 15:77,770,714 | G/A | — | uncertain significance |
| rs755249948 | 15:77,770,772 | G/C | — | uncertain significance |
| rs774069600 | 15:77,770,810 | C/T | — | uncertain significance |
| rs765517687 | 15:77,770,816 | G/A | — | uncertain significance |
| rs1175765835 | 15:77,770,834 | G/A | — | uncertain significance |
| rs1325514432 | 15:77,771,538 | A/G | — | uncertain significance |
| rs2549228079 | 15:77,771,596 | C/A | — | uncertain significance |
| rs372307524 | 15:77,771,653 | G/A | — | uncertain significance |
| rs952471 | 15:77,776,498 | C/G | 3 prime UTR variant | — |
| rs952472 | 15:77,776,562 | A/C | 3 prime UTR variant | — |
| rs7119 | 15:77,777,632 | C/T | 3 prime UTR variant | — |
| rs965480 | 15:77,781,926 | A/G | downstream gene variant | — |
| rs12910361 | 15:77,782,335 | A/G | downstream gene variant | — |
| rs8040702 | 15:77,803,615 | G/C | — | — |
| rs118151646 | 15:77,807,079 | C/T | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.