ZHX3
zinc fingers and homeoboxes 3
Summary
This gene encodes a member of the zinc fingers and homeoboxes (ZHX) gene family. The encoded protein contains two C2H2-type zinc fingers and five homeodomains and forms a dimer with itself or with zinc fingers and homeoboxes family member 1. In the nucleus, the dimerized protein interacts with the A subunit of the ubiquitous transcription factor nuclear factor-Y and may function as a transcriptional repressor. [provided by RefSeq, Jul 2008]
Known Variants155 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs4297946 | 20:39,811,275 | G/A | — | — |
| rs2664537 | 20:39,813,729 | G/A | — | benign |
| rs755245572 | 20:39,813,849 | G/A | — | likely benign |
| rs2515622186 | 20:39,813,852 | A/G | — | uncertain significance |
| rs372269518 | 20:39,813,858 | T/C | — | likely benign |
| rs78848717 | 20:39,815,697 | T/G | — | — |
| rs4344974 | 20:39,818,861 | T/C | intron variant | — |
| rs368933413 | 20:39,830,681 | C/G | — | likely benign |
| rs772367479 | 20:39,830,705 | C/T | — | uncertain significance |
| rs769247244 | 20:39,830,720 | C/A | — | uncertain significance |
| rs772725493 | 20:39,830,722 | C/T | — | likely benign |
| rs762813790 | 20:39,830,723 | G/C | — | uncertain significance |
| rs772916562 | 20:39,830,787 | A/T | — | uncertain significance |
| rs748783597 | 20:39,830,802 | T/C | — | uncertain significance |
| rs775426433 | 20:39,830,868 | T/G | — | uncertain significance |
| rs2515742991 | 20:39,830,896 | C/T | — | uncertain significance |
| rs34229622 | 20:39,830,899 | T/C | — | benign |
| rs780331804 | 20:39,830,929 | G/A | — | likely benign |
| rs771895400 | 20:39,830,999 | T/C | — | uncertain significance |
| rs374874626 | 20:39,831,018 | G/A | — | uncertain significance |
| rs2038301399 | 20:39,831,020 | T/A | — | uncertain significance |
| rs201097931 | 20:39,831,021 | T/A | — | uncertain significance |
| rs750475625 | 20:39,831,031 | A/G | — | likely benign |
| rs886301265 | 20:39,831,034 | G/A | — | likely benign |
| rs2038305158 | 20:39,831,051 | G/C | — | uncertain significance |
| rs2515744805 | 20:39,831,056 | T/C | — | uncertain significance |
| rs200260351 | 20:39,831,062 | C/T | — | uncertain significance |
| rs1437135789 | 20:39,831,075 | C/T | — | uncertain significance |
| rs752391958 | 20:39,831,076 | G/A | — | likely benign |
| rs2515745167 | 20:39,831,084 | T/G | — | uncertain significance |
| rs768520980 | 20:39,831,103 | T/C | — | likely benign |
| rs200368077 | 20:39,831,106 | G/A | — | likely benign |
| rs956414621 | 20:39,831,128 | C/T | — | uncertain significance |
| rs1201013120 | 20:39,831,185 | T/A | — | uncertain significance |
| rs373410498 | 20:39,831,231 | G/A | — | uncertain significance |
| rs781259788 | 20:39,831,267 | G/C | — | uncertain significance |
| rs199828333 | 20:39,831,295 | A/C | — | benign |
| rs147861291 | 20:39,831,308 | T/A | — | conflicting classifications of pathogenicity |
| rs577676660 | 20:39,831,315 | C/T | — | benign |
| rs34073395 | 20:39,831,348 | C/T | — | benign |
| rs2515749185 | 20:39,831,385 | G/T | — | likely benign |
| rs1025033989 | 20:39,831,393 | C/T | — | uncertain significance |
| rs865923762 | 20:39,831,398 | C/T | — | uncertain significance |
| rs149945568 | 20:39,831,407 | A/G | — | uncertain significance |
| rs200699850 | 20:39,831,448 | A/G | — | likely benign |
| rs2038353709 | 20:39,831,449 | G/C | — | uncertain significance |
| rs2038353977 | 20:39,831,450 | A/G | — | uncertain significance |
| rs777314715 | 20:39,831,467 | G/A | — | uncertain significance |
| rs2515750478 | 20:39,831,475 | C/A | — | uncertain significance |
| rs2515750530 | 20:39,831,483 | C/T | — | uncertain significance |
| rs116438906 | 20:39,831,487 | C/T | — | benign |
| rs771995478 | 20:39,831,524 | T/C | — | uncertain significance |
| rs375844415 | 20:39,831,539 | T/C | — | uncertain significance |
| rs41277006 | 20:39,831,546 | C/T | — | likely benign |
| rs2515751417 | 20:39,831,547 | C/A | — | uncertain significance |
| rs2515751463 | 20:39,831,548 | T/G | — | uncertain significance |
| rs764067657 | 20:39,831,616 | A/T | — | uncertain significance |
| rs531300412 | 20:39,831,628 | G/A | — | likely benign |
| rs201772741 | 20:39,831,700 | T/C | — | likely benign |
| rs2038380818 | 20:39,831,708 | T/C | — | uncertain significance |
| rs764944666 | 20:39,831,741 | G/A | — | uncertain significance |
| rs895167844 | 20:39,831,748 | T/C | — | likely benign |
| rs757551506 | 20:39,831,766 | G/A | — | likely benign |
| rs571516198 | 20:39,831,779 | G/A | — | uncertain significance |
| rs749654315 | 20:39,831,791 | G/A | — | uncertain significance |
| rs749788633 | 20:39,831,879 | G/T | — | uncertain significance |
| rs780486968 | 20:39,831,899 | T/A | — | uncertain significance |
| rs2515757013 | 20:39,831,925 | A/T | — | uncertain significance |
| rs1303334905 | 20:39,831,958 | G/A | — | likely benign |
| rs753020538 | 20:39,831,965 | G/A | — | uncertain significance |
| rs199728287 | 20:39,831,994 | C/G | — | uncertain significance |
| rs1217558438 | 20:39,832,116 | T/G | — | uncertain significance |
| rs765640364 | 20:39,832,133 | G/A | — | uncertain significance |
| rs202173471 | 20:39,832,136 | T/C | — | uncertain significance |
| rs752290331 | 20:39,832,158 | T/C | — | uncertain significance |
| rs771931047 | 20:39,832,209 | C/T | — | uncertain significance |
| rs746865191 | 20:39,832,214 | G/A | — | uncertain significance |
| rs35600883 | 20:39,832,242 | T/C | — | likely benign |
| rs763634799 | 20:39,832,252 | C/A | — | likely benign |
| rs370315026 | 20:39,832,310 | C/A | — | uncertain significance |
| rs763088241 | 20:39,832,317 | C/T | — | uncertain significance |
| rs140805732 | 20:39,832,318 | G/A | — | benign |
| rs144460022 | 20:39,832,328 | A/G | — | uncertain significance |
| rs375328930 | 20:39,832,342 | G/A | — | likely benign |
| rs960512306 | 20:39,832,368 | C/T | — | uncertain significance |
| rs148444276 | 20:39,832,371 | C/T | — | benign |
| rs1190498684 | 20:39,832,372 | G/A | — | likely benign |
| rs771042206 | 20:39,832,390 | C/T | — | likely benign |
| rs1229201111 | 20:39,832,421 | A/G | — | uncertain significance |
| rs142704757 | 20:39,832,427 | T/C | — | uncertain significance |
| rs1568817822 | 20:39,832,442 | C/T | — | uncertain significance |
| rs1224566475 | 20:39,832,456 | C/T | — | likely benign |
| rs41283258 | 20:39,832,495 | G/C | — | benign |
| rs2515766230 | 20:39,832,567 | G/A | — | likely benign |
| rs898085459 | 20:39,832,609 | G/C | — | uncertain significance |
| rs143152968 | 20:39,832,625 | G/A | — | uncertain significance |
| rs17265513 | 20:39,832,628 | C/T | — | benign |
| rs527915264 | 20:39,832,633 | C/T | — | likely benign |
| rs199684079 | 20:39,832,650 | G/A | — | likely benign |
| rs140288595 | 20:39,832,668 | G/C | — | uncertain significance |
Showing 100 of 155 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.