ZSWIM5
zinc finger SWIM-type containing 5
Summary
Predicted to enable zinc ion binding activity. Located in extracellular space. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants65 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs200693291 | 1:45,484,136 | C/T | — | uncertain significance |
| rs188271074 | 1:45,484,194 | C/T | — | uncertain significance |
| rs760273466 | 1:45,484,257 | T/C | — | uncertain significance |
| rs375492019 | 1:45,484,274 | T/C | — | uncertain significance |
| rs781630904 | 1:45,484,282 | G/T | — | uncertain significance |
| rs1644869383 | 1:45,484,286 | C/T | — | uncertain significance |
| rs771246734 | 1:45,484,400 | C/T | — | uncertain significance |
| rs372409844 | 1:45,484,403 | C/T | — | uncertain significance |
| rs767700654 | 1:45,484,404 | G/A | — | uncertain significance |
| rs542122003 | 1:45,484,446 | G/A | — | uncertain significance |
| rs201240018 | 1:45,484,448 | C/T | — | uncertain significance |
| rs774739657 | 1:45,484,565 | T/C | — | uncertain significance |
| rs757831548 | 1:45,484,646 | G/A | — | uncertain significance |
| rs534396669 | 1:45,484,655 | C/T | — | uncertain significance |
| rs376021528 | 1:45,484,856 | C/T | — | uncertain significance |
| rs767217345 | 1:45,484,886 | A/G | — | uncertain significance |
| rs186460547 | 1:45,484,971 | T/A | — | uncertain significance |
| rs761416742 | 1:45,485,812 | C/T | — | uncertain significance |
| rs367878283 | 1:45,486,350 | C/T | — | uncertain significance |
| rs2522982211 | 1:45,499,992 | G/C | — | uncertain significance |
| rs1322587335 | 1:45,500,044 | G/A | — | uncertain significance |
| rs767367075 | 1:45,500,055 | C/T | — | uncertain significance |
| rs757041353 | 1:45,500,065 | G/A | — | uncertain significance |
| rs2522982575 | 1:45,500,086 | T/C | — | uncertain significance |
| rs2522987178 | 1:45,501,366 | G/A | — | uncertain significance |
| rs763567594 | 1:45,501,741 | G/C | — | uncertain significance |
| rs200925379 | 1:45,501,825 | C/T | — | uncertain significance |
| rs749219790 | 1:45,501,890 | G/A | — | uncertain significance |
| rs2522990126 | 1:45,501,944 | T/A | — | uncertain significance |
| rs767873863 | 1:45,501,969 | T/C | — | uncertain significance |
| rs187838607 | 1:45,506,171 | C/T | — | uncertain significance |
| rs534597963 | 1:45,508,950 | G/A | — | uncertain significance |
| rs554565025 | 1:45,508,959 | G/A | — | uncertain significance |
| rs1040781904 | 1:45,508,960 | T/C | — | uncertain significance |
| rs199535486 | 1:45,509,001 | T/C | — | uncertain significance |
| rs376331512 | 1:45,509,046 | C/T | — | uncertain significance |
| rs2523011427 | 1:45,509,052 | G/A | — | uncertain significance |
| rs2523040757 | 1:45,516,823 | G/C | — | uncertain significance |
| rs546087330 | 1:45,524,305 | A/G | — | uncertain significance |
| rs77616762 | 1:45,524,311 | C/T | — | benign |
| rs777495038 | 1:45,524,395 | C/G | — | uncertain significance |
| rs770229441 | 1:45,525,787 | T/C | — | likely benign |
| rs368896573 | 1:45,525,833 | G/A | — | uncertain significance |
| rs754577245 | 1:45,553,570 | T/G | — | uncertain significance |
| rs369736457 | 1:45,553,636 | G/T | — | uncertain significance |
| rs1645341941 | 1:45,553,684 | T/C | — | uncertain significance |
| rs374367203 | 1:45,553,711 | C/T | — | uncertain significance |
| rs200296228 | 1:45,553,735 | C/T | — | uncertain significance |
| rs1645342525 | 1:45,553,769 | C/A | — | uncertain significance |
| rs375121620 | 1:45,553,825 | C/T | — | uncertain significance |
| rs2523149958 | 1:45,553,909 | C/T | — | uncertain significance |
| rs141862131 | 1:45,571,797 | T/C | intron variant | — |
| rs2523458225 | 1:45,671,479 | G/A | — | uncertain significance |
| rs377119690 | 1:45,671,527 | C/A | — | uncertain significance |
| rs1646186302 | 1:45,671,568 | G/A | — | uncertain significance |
| rs2523459054 | 1:45,671,586 | G/C | — | uncertain significance |
| rs1312850830 | 1:45,671,602 | G/A | — | uncertain significance |
| rs1646187015 | 1:45,671,625 | G/A | — | uncertain significance |
| rs2149059772 | 1:45,671,626 | A/G | — | uncertain significance |
| rs772131026 | 1:45,671,632 | C/T | — | uncertain significance |
| rs1646188411 | 1:45,671,760 | C/T | — | uncertain significance |
| rs1379065031 | 1:45,671,781 | C/T | — | uncertain significance |
| rs2523461139 | 1:45,671,917 | A/G | — | uncertain significance |
| rs2523461258 | 1:45,671,934 | G/A | — | uncertain significance |
| rs1043855942 | 1:45,671,992 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.