PHF19
PHD finger protein 19
Summary
Enables methylated histone binding activity. Involved in negative regulation of gene expression, epigenetic. Located in ESC/E(Z) complex. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants29 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2045398283 | 9:123,620,303 | C/G | — | uncertain significance |
| rs2045398598 | 9:123,620,325 | C/T | — | uncertain significance |
| rs767617200 | 9:123,620,518 | T/A | — | uncertain significance |
| rs2045565913 | 9:123,624,887 | T/C | — | uncertain significance |
| rs150134029 | 9:123,624,890 | C/T | — | uncertain significance |
| rs746842572 | 9:123,624,975 | T/C | — | uncertain significance |
| rs2540215949 | 9:123,624,994 | C/G | — | uncertain significance |
| rs769328755 | 9:123,625,006 | G/C | — | uncertain significance |
| rs763051589 | 9:123,628,044 | A/G | — | uncertain significance |
| rs774410769 | 9:123,628,325 | C/T | — | uncertain significance |
| rs562189531 | 9:123,629,161 | T/A | — | uncertain significance |
| rs1311999170 | 9:123,629,232 | C/T | — | uncertain significance |
| rs7847628 | 9:123,631,225 | A/C | — | — |
| rs139838568 | 9:123,631,528 | C/G | — | uncertain significance |
| rs200127495 | 9:123,632,137 | C/T | — | uncertain significance |
| rs907039928 | 9:123,632,200 | G/T | — | uncertain significance |
| rs151197147 | 9:123,632,759 | G/A | — | uncertain significance |
| rs763071504 | 9:123,632,768 | G/A | — | uncertain significance |
| rs1358206029 | 9:123,632,783 | A/T | — | uncertain significance |
| rs1378190642 | 9:123,632,793 | T/G | — | uncertain significance |
| rs4836833 | 9:123,632,829 | G/A | intron variant | — |
| rs10985070 | 9:123,636,121 | C/A | regulatory region variant | — |
| rs1953126 | 9:123,640,500 | T/C | regulatory region variant | — |
| rs7858209 | 9:123,645,760 | G/A | intergenic variant | — |
| rs10818483 | 9:123,650,473 | T/C | intergenic variant | — |
| rs10760123 | 9:123,650,534 | T/G | intergenic variant | — |
| rs2072438 | 9:123,651,301 | T/C | intergenic variant | — |
| rs881375 | 9:123,652,898 | T/C | regulatory region variant | — |
| rs10760126 | 9:123,662,618 | T/C | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.