ZNF516
zinc finger protein 516
Summary
Zinc-finger proteins bind nucleic acids and play important roles in various cellular functions, including cell proliferation, differentiation, and apoptosis. This gene encodes a zinc-finger protein, and belongs to the krueppel C2H2-type zinc-finger protein family. It may be involved in transcriptional regulation. [provided by RefSeq, Sep 2012]
Known Variants115 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs590218 | 18:74,069,883 | G/C | — | — |
| rs1047922 | 18:74,070,562 | T/C | 3 prime UTR variant | — |
| rs72973714 | 18:74,076,020 | C/T | intron variant | — |
| rs762133977 | 18:74,090,855 | G/T | — | uncertain significance |
| rs748871555 | 18:74,090,966 | G/A | — | uncertain significance |
| rs200905294 | 18:74,090,976 | C/T | — | uncertain significance |
| rs374668991 | 18:74,091,004 | G/A | — | likely benign |
| rs754664969 | 18:74,091,014 | C/A | — | uncertain significance |
| rs1418686194 | 18:74,091,041 | A/G | — | uncertain significance |
| rs774619084 | 18:74,091,048 | G/T | — | uncertain significance |
| rs372078590 | 18:74,091,071 | C/T | — | uncertain significance |
| rs369778017 | 18:74,091,090 | C/T | — | uncertain significance |
| rs375660551 | 18:74,091,157 | C/T | — | likely benign |
| rs775101945 | 18:74,091,176 | G/C | — | uncertain significance |
| rs1254606711 | 18:74,091,224 | G/A | — | uncertain significance |
| rs2511995854 | 18:74,091,246 | G/C | — | uncertain significance |
| rs370362208 | 18:74,091,275 | G/A | — | uncertain significance |
| rs367565077 | 18:74,091,308 | C/T | — | uncertain significance |
| rs755006051 | 18:74,091,325 | T/G | — | uncertain significance |
| rs746595310 | 18:74,091,350 | T/G | — | uncertain significance |
| rs533469182 | 18:74,091,364 | C/G | — | uncertain significance |
| rs1231884564 | 18:74,091,371 | G/A | — | uncertain significance |
| rs192324175 | 18:74,091,444 | C/A | — | conflicting classifications of pathogenicity |
| rs2511998356 | 18:74,091,447 | A/G | — | uncertain significance |
| rs1837801758 | 18:74,091,463 | G/T | — | uncertain significance |
| rs959594851 | 18:74,091,467 | T/C | — | uncertain significance |
| rs777017774 | 18:74,091,489 | C/T | — | uncertain significance |
| rs748518575 | 18:74,091,560 | C/T | — | uncertain significance |
| rs781760407 | 18:74,091,656 | C/T | — | likely benign |
| rs1325253141 | 18:74,091,674 | C/T | — | uncertain significance |
| rs541868634 | 18:74,091,677 | T/C | — | uncertain significance |
| rs1467899925 | 18:74,091,707 | T/C | — | likely benign |
| rs781764706 | 18:74,091,710 | C/T | — | uncertain significance |
| rs778990580 | 18:74,091,732 | G/A | — | uncertain significance |
| rs373304915 | 18:74,091,768 | T/C | — | uncertain significance |
| rs1599149539 | 18:74,091,806 | G/A | — | uncertain significance |
| rs369474214 | 18:74,091,818 | G/A | — | uncertain significance |
| rs758595599 | 18:74,091,828 | C/T | — | uncertain significance |
| rs200255972 | 18:74,091,834 | T/C | — | uncertain significance |
| rs1033724094 | 18:74,091,857 | C/T | — | uncertain significance |
| rs760936274 | 18:74,091,878 | A/G | — | uncertain significance |
| rs748455883 | 18:74,091,882 | G/A | — | uncertain significance |
| rs531158367 | 18:74,091,897 | C/T | — | uncertain significance |
| rs569479817 | 18:74,091,914 | G/A | — | uncertain significance |
| rs774090688 | 18:74,091,918 | G/A | — | uncertain significance |
| rs1304511784 | 18:74,091,943 | C/A | — | uncertain significance |
| rs201679855 | 18:74,091,962 | G/A | — | likely benign |
| rs780129703 | 18:74,091,980 | G/A | — | uncertain significance |
| rs368813175 | 18:74,092,014 | C/T | — | uncertain significance |
| rs889642077 | 18:74,092,124 | G/C | — | uncertain significance |
| rs559748313 | 18:74,092,152 | C/T | — | likely benign |
| rs200573902 | 18:74,092,170 | C/A | — | uncertain significance |
| rs201694420 | 18:74,092,203 | T/C | — | uncertain significance |
| rs542430571 | 18:74,092,244 | C/T | — | likely benign |
| rs373968169 | 18:74,092,247 | C/T | — | likely benign |
| rs368128166 | 18:74,092,248 | G/A | — | uncertain significance |
| rs371757743 | 18:74,092,250 | G/A | — | uncertain significance |
| rs4891159 | 18:74,101,941 | G/A | intron variant | — |
| rs112984554 | 18:74,141,327 | G/A | intron variant | — |
| rs114279579 | 18:74,153,258 | G/A | — | benign |
| rs201517734 | 18:74,153,287 | C/T | — | uncertain significance |
| rs780359683 | 18:74,153,291 | C/T | — | uncertain significance |
| rs2512325230 | 18:74,153,315 | A/T | — | uncertain significance |
| rs569947953 | 18:74,153,320 | G/C | — | uncertain significance |
| rs2512325474 | 18:74,153,333 | T/G | — | uncertain significance |
| rs762206848 | 18:74,153,348 | G/A | — | uncertain significance |
| rs750858645 | 18:74,153,353 | C/T | — | uncertain significance |
| rs377762530 | 18:74,153,366 | C/T | — | uncertain significance |
| rs941297055 | 18:74,153,428 | T/C | — | uncertain significance |
| rs2512327763 | 18:74,153,501 | T/C | — | uncertain significance |
| rs777057785 | 18:74,153,509 | G/T | — | uncertain significance |
| rs2512328177 | 18:74,153,531 | C/G | — | uncertain significance |
| rs891504348 | 18:74,153,548 | G/A | — | uncertain significance |
| rs971179022 | 18:74,153,593 | G/A | — | uncertain significance |
| rs778571913 | 18:74,153,594 | C/T | — | uncertain significance |
| rs764224329 | 18:74,153,651 | G/A | — | uncertain significance |
| rs558532980 | 18:74,153,743 | G/A | — | uncertain significance |
| rs776257877 | 18:74,153,839 | G/A | — | uncertain significance |
| rs745591863 | 18:74,153,915 | G/T | — | uncertain significance |
| rs754247710 | 18:74,153,947 | G/T | — | uncertain significance |
| rs1252826711 | 18:74,153,957 | C/T | — | uncertain significance |
| rs201724798 | 18:74,154,070 | G/A | — | uncertain significance |
| rs199570810 | 18:74,154,089 | G/T | — | uncertain significance |
| rs1172742819 | 18:74,154,106 | G/A | — | uncertain significance |
| rs7233640 | 18:74,154,141 | G/A | — | benign |
| rs1911718416 | 18:74,154,228 | C/G | — | uncertain significance |
| rs765438860 | 18:74,154,323 | C/T | — | uncertain significance |
| rs374622201 | 18:74,154,328 | C/T | — | uncertain significance |
| rs757228995 | 18:74,154,331 | T/C | — | uncertain significance |
| rs765406110 | 18:74,154,391 | T/A | — | uncertain significance |
| rs1177982089 | 18:74,154,424 | G/A | — | uncertain significance |
| rs2512338802 | 18:74,154,430 | T/C | — | uncertain significance |
| rs779596444 | 18:74,154,434 | C/T | — | uncertain significance |
| rs554066909 | 18:74,154,467 | G/T | — | likely benign |
| rs1192667899 | 18:74,154,475 | C/A | — | uncertain significance |
| rs556333796 | 18:74,154,512 | G/A | — | uncertain significance |
| rs572758212 | 18:74,154,536 | C/G | — | uncertain significance |
| rs1911767834 | 18:74,154,592 | A/G | — | uncertain significance |
| rs762650409 | 18:74,154,616 | G/A | — | uncertain significance |
| rs766933381 | 18:74,154,622 | C/T | — | uncertain significance |
Showing 100 of 115 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.