ZNF503
zinc finger protein 503
Summary
Predicted to enable zinc ion binding activity. Involved in G1 to G0 transition involved in cell differentiation; negative regulation of cell population proliferation; and negative regulation of gene expression. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants46 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs568971618 | 10:77,149,808 | C/T | — | — |
| rs1053391 | 10:77,158,588 | G/A | — | likely benign |
| rs371070869 | 10:77,158,622 | G/A | — | uncertain significance |
| rs2492316045 | 10:77,158,674 | G/T | — | uncertain significance |
| rs2492316162 | 10:77,158,697 | G/A | — | uncertain significance |
| rs202007168 | 10:77,158,710 | C/T | — | uncertain significance |
| rs1475703418 | 10:77,158,731 | T/C | — | uncertain significance |
| rs111641846 | 10:77,158,778 | C/G | — | uncertain significance |
| rs1340151438 | 10:77,158,830 | G/C | — | uncertain significance |
| rs35764982 | 10:77,158,921 | G/C | — | uncertain significance |
| rs1206280988 | 10:77,159,000 | G/A | — | uncertain significance |
| rs201443753 | 10:77,159,048 | G/A | — | uncertain significance |
| rs1043313899 | 10:77,159,102 | G/A | — | uncertain significance |
| rs1487991767 | 10:77,159,120 | C/A | — | uncertain significance |
| rs1216992767 | 10:77,159,274 | C/A | — | uncertain significance |
| rs761194053 | 10:77,159,330 | T/C | — | uncertain significance |
| rs940910771 | 10:77,159,496 | T/C | — | uncertain significance |
| rs973627326 | 10:77,159,501 | C/A | — | uncertain significance |
| rs61743304 | 10:77,159,503 | C/T | — | benign |
| rs760226690 | 10:77,159,546 | C/T | — | uncertain significance |
| rs370967290 | 10:77,159,558 | T/A | — | uncertain significance |
| rs1396064945 | 10:77,159,573 | A/C | — | uncertain significance |
| rs377695668 | 10:77,159,639 | G/T | — | uncertain significance |
| rs1228664722 | 10:77,159,652 | C/A | — | uncertain significance |
| rs756201269 | 10:77,159,675 | G/T | — | uncertain significance |
| rs894393092 | 10:77,159,681 | T/G | — | uncertain significance |
| rs1207921871 | 10:77,159,708 | C/A | — | uncertain significance |
| rs1222551382 | 10:77,159,750 | G/A | — | uncertain significance |
| rs200297480 | 10:77,159,751 | C/G | — | uncertain significance |
| rs747667090 | 10:77,159,782 | G/C | — | uncertain significance |
| rs2492322428 | 10:77,159,829 | A/T | — | uncertain significance |
| rs1245260674 | 10:77,159,847 | C/A | — | uncertain significance |
| rs1843770511 | 10:77,159,904 | C/T | — | uncertain significance |
| rs554497686 | 10:77,159,906 | G/T | — | uncertain significance |
| rs907056025 | 10:77,159,937 | C/A | — | uncertain significance |
| rs1331719892 | 10:77,159,960 | T/C | — | uncertain significance |
| rs766507366 | 10:77,160,028 | G/C | — | uncertain significance |
| rs1843805613 | 10:77,160,985 | G/A | — | uncertain significance |
| rs994168143 | 10:77,160,988 | C/T | — | uncertain significance |
| rs935115439 | 10:77,161,048 | C/T | — | uncertain significance |
| rs375353140 | 10:77,161,059 | C/G | — | uncertain significance |
| rs767771319 | 10:77,161,085 | G/A | — | likely benign |
| rs548026488 | 10:77,161,087 | C/G | — | uncertain significance |
| rs764097121 | 10:77,161,089 | G/C | — | uncertain significance |
| rs2492328576 | 10:77,161,099 | C/T | — | uncertain significance |
| rs956436529 | 10:77,161,135 | G/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.