PHF21B
PHD finger protein 21B
Summary
Predicted to enable zinc ion binding activity. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants28 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs759574568 | 22:45,279,073 | C/T | — | uncertain significance |
| rs2070769083 | 22:45,279,109 | G/C | — | uncertain significance |
| rs995230586 | 22:45,279,127 | G/C | — | uncertain significance |
| rs753448825 | 22:45,281,319 | G/A | — | uncertain significance |
| rs746179699 | 22:45,281,328 | C/T | — | uncertain significance |
| rs759215827 | 22:45,283,881 | G/C | — | uncertain significance |
| rs2518659759 | 22:45,283,914 | G/A | — | uncertain significance |
| rs61739200 | 22:45,283,971 | C/A | — | uncertain significance |
| rs749238504 | 22:45,283,987 | G/C | — | uncertain significance |
| rs2070927733 | 22:45,285,643 | C/G | — | uncertain significance |
| rs574600247 | 22:45,287,191 | G/A | — | uncertain significance |
| rs771465645 | 22:45,287,227 | G/A | — | uncertain significance |
| rs199983690 | 22:45,309,788 | G/A | — | uncertain significance |
| rs201312214 | 22:45,309,808 | G/A | — | uncertain significance |
| rs753284224 | 22:45,309,814 | G/A | — | uncertain significance |
| rs748056039 | 22:45,309,857 | G/A | — | uncertain significance |
| rs578214624 | 22:45,309,946 | G/A | — | uncertain significance |
| rs760468264 | 22:45,312,219 | C/T | — | uncertain significance |
| rs781408802 | 22:45,312,237 | T/C | — | uncertain significance |
| rs140879621 | 22:45,312,410 | C/T | — | uncertain significance |
| rs2518733459 | 22:45,312,417 | C/T | — | uncertain significance |
| rs983447409 | 22:45,312,446 | T/C | — | uncertain significance |
| rs749050347 | 22:45,312,461 | C/T | — | uncertain significance |
| rs369146125 | 22:45,316,304 | C/T | — | uncertain significance |
| rs8141413 | 22:45,337,393 | T/C | intron variant | — |
| rs2073369343 | 22:45,404,481 | A/C | — | uncertain significance |
| rs943495792 | 22:45,405,408 | T/G | — | uncertain significance |
| rs1243966930 | 22:45,405,419 | C/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.