ZNF831
zinc finger protein 831
Summary
Predicted to enable zinc ion binding activity. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants153 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs236717 | 20:57,701,654 | G/A | intergenic variant | — |
| rs558916355 | 20:57,708,414 | C/T | — | — |
| rs77044088 | 20:57,711,098 | C/G | intergenic variant | — |
| rs77168628 | 20:57,712,284 | T/A | intergenic variant | — |
| rs260020 | 20:57,714,025 | C/G | — | — |
| rs78953748 | 20:57,715,798 | T/G | intergenic variant | — |
| rs74729242 | 20:57,718,690 | T/C | intergenic variant | — |
| rs6026729 | 20:57,728,269 | C/T | intergenic variant | — |
| rs75245746 | 20:57,730,418 | T/C | intergenic variant | — |
| rs11906755 | 20:57,733,334 | A/G | intergenic variant | — |
| rs78302204 | 20:57,735,448 | G/A | intergenic variant | — |
| rs536403690 | 20:57,736,363 | C/T | — | — |
| rs73306876 | 20:57,739,829 | A/G | intergenic variant | — |
| rs6026740 | 20:57,740,348 | A/T | — | — |
| rs6026744 | 20:57,742,388 | A/T | intergenic variant | — |
| rs11906149 | 20:57,744,869 | G/A | — | — |
| rs11908189 | 20:57,744,871 | T/C | intergenic variant | — |
| rs79263055 | 20:57,750,478 | T/C | — | — |
| rs73306896 | 20:57,750,533 | C/T | intergenic variant | — |
| rs6015450 | 20:57,751,117 | A/G | intergenic variant | — |
| rs141230198 | 20:57,752,721 | T/G | intergenic variant | — |
| rs74715624 | 20:57,753,203 | T/G | — | — |
| rs16982520 | 20:57,758,720 | A/G | intergenic variant | — |
| rs12480733 | 20:57,761,681 | G/T | upstream gene variant | — |
| rs774065552 | 20:57,766,151 | C/T | — | uncertain significance |
| rs1453419677 | 20:57,766,180 | A/T | — | uncertain significance |
| rs753778394 | 20:57,766,220 | C/T | — | uncertain significance |
| rs61742487 | 20:57,766,221 | C/A | — | benign |
| rs768309081 | 20:57,766,225 | C/T | — | uncertain significance |
| rs575210641 | 20:57,766,226 | C/A | — | uncertain significance |
| rs2146543963 | 20:57,766,247 | T/C | — | uncertain significance |
| rs778876349 | 20:57,766,268 | C/T | — | uncertain significance |
| rs558289892 | 20:57,766,294 | C/G | — | uncertain significance |
| rs764029741 | 20:57,766,321 | G/C | — | uncertain significance |
| rs749815984 | 20:57,766,372 | C/T | — | uncertain significance |
| rs201880381 | 20:57,766,460 | G/A | — | uncertain significance |
| rs143620250 | 20:57,766,466 | C/G | — | uncertain significance |
| rs778067509 | 20:57,766,679 | T/C | — | uncertain significance |
| rs1443345757 | 20:57,766,702 | G/A | — | uncertain significance |
| rs1210778443 | 20:57,766,738 | G/C | — | uncertain significance |
| rs754923619 | 20:57,766,871 | C/T | — | likely benign |
| rs777486723 | 20:57,766,889 | C/A | — | uncertain significance |
| rs563255417 | 20:57,766,937 | C/T | — | benign |
| rs756033182 | 20:57,766,985 | A/G | — | uncertain significance |
| rs564350771 | 20:57,767,041 | G/A | — | uncertain significance |
| rs753668194 | 20:57,767,051 | C/T | — | uncertain significance |
| rs2146559750 | 20:57,767,153 | G/A | — | uncertain significance |
| rs779827121 | 20:57,767,159 | C/A | — | uncertain significance |
| rs770198523 | 20:57,767,197 | G/T | — | uncertain significance |
| rs113266043 | 20:57,767,244 | C/T | — | likely benign |
| rs200797810 | 20:57,767,371 | G/A | — | uncertain significance |
| rs201993964 | 20:57,767,398 | C/A | — | uncertain significance |
| rs200610922 | 20:57,767,433 | C/T | — | likely benign |
| rs1470936579 | 20:57,767,471 | C/A | — | uncertain significance |
| rs2146568181 | 20:57,767,648 | C/G | — | uncertain significance |
| rs767929048 | 20:57,767,660 | C/A | — | uncertain significance |
| rs1983683558 | 20:57,767,669 | C/T | — | uncertain significance |
| rs114604989 | 20:57,767,687 | G/A | — | benign |
| rs746879362 | 20:57,767,695 | C/T | — | uncertain significance |
| rs757389056 | 20:57,767,746 | C/A | — | uncertain significance |
| rs778790344 | 20:57,767,749 | C/T | — | uncertain significance |
| rs61743783 | 20:57,767,817 | C/T | — | benign |
| rs552086601 | 20:57,767,838 | G/T | — | uncertain significance |
| rs144506912 | 20:57,767,873 | G/A | — | uncertain significance |
| rs776168252 | 20:57,767,921 | C/T | — | uncertain significance |
| rs182458619 | 20:57,767,943 | C/T | — | benign |
| rs61743782 | 20:57,767,960 | A/G | — | benign |
| rs778725917 | 20:57,767,962 | A/G | — | uncertain significance |
| rs2516103168 | 20:57,767,965 | A/T | — | uncertain significance |
| rs2516103735 | 20:57,768,007 | G/T | — | uncertain significance |
| rs1220058577 | 20:57,768,094 | C/G | — | uncertain significance |
| rs367968831 | 20:57,768,116 | A/G | — | uncertain significance |
| rs1983747620 | 20:57,768,137 | C/A | — | uncertain significance |
| rs765181998 | 20:57,768,175 | G/A | — | uncertain significance |
| rs61742495 | 20:57,768,239 | G/A | — | likely benign |
| rs61743781 | 20:57,768,417 | G/A | — | benign |
| rs1000920918 | 20:57,768,425 | A/G | — | uncertain significance |
| rs760261090 | 20:57,768,514 | G/C | — | uncertain significance |
| rs57571629 | 20:57,768,531 | C/T | — | benign |
| rs1983797598 | 20:57,768,573 | G/C | — | uncertain significance |
| rs558775656 | 20:57,768,661 | G/A | — | uncertain significance |
| rs1489584400 | 20:57,768,668 | T/C | — | uncertain significance |
| rs2146587033 | 20:57,768,706 | G/A | — | uncertain significance |
| rs545387355 | 20:57,768,712 | C/A | — | uncertain significance |
| rs2146588294 | 20:57,768,782 | C/A | — | uncertain significance |
| rs2146588366 | 20:57,768,787 | C/A | — | uncertain significance |
| rs776861312 | 20:57,768,841 | C/T | — | uncertain significance |
| rs1983831448 | 20:57,768,855 | A/C | — | uncertain significance |
| rs531807718 | 20:57,768,887 | C/T | — | uncertain significance |
| rs568943919 | 20:57,768,919 | G/A | — | uncertain significance |
| rs368553201 | 20:57,768,923 | C/A | — | uncertain significance |
| rs373788780 | 20:57,768,956 | G/T | — | uncertain significance |
| rs202026682 | 20:57,769,001 | G/A | — | likely benign |
| rs199744168 | 20:57,769,003 | G/T | — | uncertain significance |
| rs1983867343 | 20:57,769,154 | G/C | — | uncertain significance |
| rs749543585 | 20:57,769,180 | G/A | — | uncertain significance |
| rs776712812 | 20:57,769,211 | G/A | — | uncertain significance |
| rs748038835 | 20:57,769,213 | G/A | — | uncertain significance |
| rs372829780 | 20:57,769,250 | C/T | — | likely benign |
| rs943482294 | 20:57,769,262 | A/C | — | uncertain significance |
Showing 100 of 153 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.