PHF20
PHD finger protein 20
Summary
Predicted to enable DNA binding activity and zinc ion binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in cytosol; nuclear membrane; and nucleoplasm. Part of MLL1 complex and NSL complex. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants56 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs150116001 | 20:34,370,184 | G/T | — | — |
| rs539279872 | 20:34,372,309 | C/G | — | — |
| rs11906854 | 20:34,383,634 | A/G | intron variant | — |
| rs768125992 | 20:34,389,515 | G/A | — | uncertain significance |
| rs6119655 | 20:34,412,049 | G/A | regulatory region variant | — |
| rs112103450 | 20:34,415,578 | T/G | — | — |
| rs2425157 | 20:34,419,083 | T/C | regulatory region variant | — |
| rs2425158 | 20:34,419,664 | T/C | intron variant | — |
| rs2425161 | 20:34,427,192 | A/T | — | — |
| rs2515954250 | 20:34,430,598 | C/T | — | uncertain significance |
| rs2425163 | 20:34,432,670 | A/T | — | — |
| rs756903137 | 20:34,435,333 | A/G | — | uncertain significance |
| rs200034859 | 20:34,446,298 | G/C | — | uncertain significance |
| rs79291837 | 20:34,451,162 | C/T | — | benign |
| rs1014731601 | 20:34,451,218 | C/A | — | uncertain significance |
| rs2515995461 | 20:34,451,259 | C/T | — | uncertain significance |
| rs6060648 | 20:34,456,704 | A/G | intron variant | — |
| rs2516008986 | 20:34,457,368 | T/C | — | uncertain significance |
| rs1456887132 | 20:34,457,441 | C/T | — | likely pathogenic |
| rs1458945046 | 20:34,458,901 | C/T | — | uncertain significance |
| rs368676517 | 20:34,459,009 | C/T | — | uncertain significance |
| rs750898682 | 20:34,459,604 | G/T | — | uncertain significance |
| rs1036855912 | 20:34,459,637 | G/C | — | uncertain significance |
| rs200469725 | 20:34,459,679 | A/G | — | uncertain significance |
| rs369867507 | 20:34,459,707 | C/T | — | uncertain significance |
| rs750250426 | 20:34,459,718 | C/G | — | uncertain significance |
| rs2516092135 | 20:34,487,470 | G/C | — | uncertain significance |
| rs35658867 | 20:34,487,478 | G/A | — | uncertain significance |
| rs1266938951 | 20:34,487,531 | G/C | — | uncertain significance |
| rs113416762 | 20:34,494,389 | C/T | intron variant | — |
| rs779220829 | 20:34,501,213 | A/T | — | uncertain significance |
| rs527952040 | 20:34,502,066 | C/T | — | uncertain significance |
| rs139713561 | 20:34,505,397 | T/G | — | benign |
| rs73618547 | 20:34,505,402 | G/A | — | benign |
| rs1033152132 | 20:34,505,406 | A/T | — | uncertain significance |
| rs144394347 | 20:34,505,443 | T/C | — | benign |
| rs370502808 | 20:34,505,511 | G/A | — | uncertain significance |
| rs2055747305 | 20:34,519,206 | G/A | — | uncertain significance |
| rs34576397 | 20:34,519,284 | G/A | — | uncertain significance |
| rs751554371 | 20:34,519,329 | G/A | — | uncertain significance |
| rs2516187229 | 20:34,526,631 | T/A | — | uncertain significance |
| rs555729193 | 20:34,526,671 | T/G | — | uncertain significance |
| rs574165917 | 20:34,526,672 | C/T | — | uncertain significance |
| rs36058204 | 20:34,526,720 | G/C | — | benign |
| rs149353721 | 20:34,526,799 | G/A | — | benign |
| rs144252568 | 20:34,526,851 | C/T | — | uncertain significance |
| rs17347322 | 20:34,526,853 | T/C | — | benign |
| rs1325679393 | 20:34,526,903 | C/T | — | uncertain significance |
| rs771829423 | 20:34,526,911 | G/A | — | likely pathogenic |
| rs200315522 | 20:34,526,918 | C/T | — | uncertain significance |
| rs181763739 | 20:34,526,960 | C/T | — | uncertain significance |
| rs1303091960 | 20:34,526,990 | G/A | — | uncertain significance |
| rs61738923 | 20:34,528,794 | A/G | — | benign |
| rs140445450 | 20:34,535,401 | C/T | — | likely benign |
| rs1371531251 | 20:34,535,444 | G/C | — | uncertain significance |
| rs775261403 | 20:34,535,469 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.