ZFAND4
zinc finger AN1-type containing 4
Summary
Predicted to enable zinc ion binding activity. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants55 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs183419581 | 10:46,110,574 | A/G | downstream gene variant | — |
| rs202137114 | 10:46,111,922 | T/C | — | uncertain significance |
| rs759964148 | 10:46,111,928 | C/T | — | uncertain significance |
| rs2044955608 | 10:46,111,979 | T/C | — | uncertain significance |
| rs2493769761 | 10:46,112,014 | C/T | — | uncertain significance |
| rs531442923 | 10:46,113,619 | T/C | — | uncertain significance |
| rs1465019972 | 10:46,113,663 | T/C | — | uncertain significance |
| rs199505728 | 10:46,118,361 | G/A | — | — |
| rs1352413938 | 10:46,120,039 | T/C | — | uncertain significance |
| rs141515378 | 10:46,121,401 | A/C | — | uncertain significance |
| rs749776780 | 10:46,121,422 | A/T | — | uncertain significance |
| rs757776951 | 10:46,121,423 | C/A | — | uncertain significance |
| rs768474616 | 10:46,121,430 | G/C | — | uncertain significance |
| rs149725835 | 10:46,121,548 | C/T | — | likely benign |
| rs759425309 | 10:46,121,559 | G/T | — | uncertain significance |
| rs765370078 | 10:46,121,611 | T/A | — | uncertain significance |
| rs942955327 | 10:46,121,662 | T/C | — | uncertain significance |
| rs535799989 | 10:46,121,703 | G/A | — | uncertain significance |
| rs202064320 | 10:46,121,797 | T/C | — | uncertain significance |
| rs745377255 | 10:46,121,826 | G/A | — | uncertain significance |
| rs376569146 | 10:46,121,835 | G/A | — | uncertain significance |
| rs141032179 | 10:46,121,838 | G/T | — | uncertain significance |
| rs372234665 | 10:46,121,845 | G/A | — | uncertain significance |
| rs41299230 | 10:46,121,886 | T/C | — | likely benign |
| rs2493914601 | 10:46,122,070 | G/C | — | uncertain significance |
| rs186385354 | 10:46,122,120 | G/A | — | uncertain significance |
| rs372955633 | 10:46,122,205 | C/T | — | uncertain significance |
| rs1450709281 | 10:46,122,219 | T/C | — | uncertain significance |
| rs760757010 | 10:46,122,226 | C/T | — | uncertain significance |
| rs373232001 | 10:46,122,267 | A/G | — | uncertain significance |
| rs764132017 | 10:46,122,305 | G/C | — | uncertain significance |
| rs185125387 | 10:46,122,369 | G/A | — | uncertain significance |
| rs201953415 | 10:46,122,384 | A/T | — | uncertain significance |
| rs1201602833 | 10:46,122,526 | G/A | — | uncertain significance |
| rs76721209 | 10:46,126,767 | A/C | — | — |
| rs772220262 | 10:46,135,277 | T/C | — | uncertain significance |
| rs1056255239 | 10:46,135,312 | C/G | — | uncertain significance |
| rs201853061 | 10:46,135,316 | T/A | — | uncertain significance |
| rs758823456 | 10:46,135,320 | T/C | — | uncertain significance |
| rs777335661 | 10:46,135,355 | G/C | — | uncertain significance |
| rs143924829 | 10:46,135,376 | T/C | — | uncertain significance |
| rs771922152 | 10:46,135,377 | C/G | — | uncertain significance |
| rs199995795 | 10:46,135,407 | C/G | — | uncertain significance |
| rs761953293 | 10:46,135,409 | C/T | — | uncertain significance |
| rs140671460 | 10:46,143,767 | G/A | — | uncertain significance |
| rs2494263968 | 10:46,143,824 | T/C | — | uncertain significance |
| rs573366778 | 10:46,143,826 | C/T | — | uncertain significance |
| rs145327982 | 10:46,143,861 | T/G | — | uncertain significance |
| rs2047543457 | 10:46,143,937 | G/A | — | uncertain significance |
| rs2047543632 | 10:46,143,939 | A/T | — | uncertain significance |
| rs1589392156 | 10:46,148,456 | T/C | — | uncertain significance |
| rs186530989 | 10:46,156,188 | T/G | — | — |
| rs2048619975 | 10:46,159,100 | C/A | — | uncertain significance |
| rs143802814 | 10:46,159,116 | A/G | — | uncertain significance |
| rs140527381 | 10:46,168,998 | C/G | upstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.