ZFAND3
zinc finger AN1-type containing 3
Summary
Predicted to enable DNA binding activity and zinc ion binding activity. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants31 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2481030222 | 6:37,787,732 | C/A | — | uncertain significance |
| rs1763629787 | 6:37,787,758 | A/T | — | uncertain significance |
| rs259720 | 6:37,791,578 | G/T | upstream gene variant | — |
| rs183620696 | 6:37,801,558 | C/T | upstream gene variant | — |
| rs536809595 | 6:37,839,912 | T/G | — | — |
| rs186186238 | 6:37,850,782 | G/A | regulatory region variant | — |
| rs565190590 | 6:37,854,004 | A/G | — | — |
| rs191792572 | 6:37,859,607 | C/T | intron variant | — |
| rs3852216 | 6:37,874,971 | A/G | intron variant | — |
| rs567371507 | 6:37,885,884 | G/T | — | — |
| rs141076248 | 6:37,940,707 | A/G | intron variant | — |
| rs554465524 | 6:37,951,306 | T/C | — | — |
| rs72850884 | 6:37,964,338 | T/C | intron variant | — |
| rs77581126 | 6:37,974,141 | C/T | upstream gene variant | — |
| rs577927897 | 6:37,979,175 | C/T | — | — |
| rs190036926 | 6:37,979,959 | G/A | intron variant | — |
| rs2645094 | 6:37,982,112 | T/A | — | — |
| rs116387621 | 6:37,990,107 | G/C | intron variant | — |
| rs553460173 | 6:38,028,070 | A/G | — | — |
| rs752699733 | 6:38,029,392 | G/A | — | uncertain significance |
| rs1260264472 | 6:38,029,444 | A/G | — | uncertain significance |
| rs767635275 | 6:38,029,513 | C/T | — | uncertain significance |
| rs771830587 | 6:38,029,543 | A/G | — | uncertain significance |
| rs17589516 | 6:38,036,420 | A/G | intron variant | — |
| rs57374526 | 6:38,049,933 | G/T | — | — |
| rs7452628 | 6:38,071,178 | T/C | — | — |
| rs576880607 | 6:38,080,263 | C/T | — | — |
| rs1210218675 | 6:38,084,377 | G/A | — | uncertain significance |
| rs1025679313 | 6:38,084,411 | G/A | — | uncertain significance |
| rs2532506031 | 6:38,084,474 | A/G | — | uncertain significance |
| rs9470794 | 6:38,106,844 | T/C | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.