ZNF804A
zinc finger protein 804A
Summary
The protein encoded by this gene is a zinc finger binding protein. Polymorphisms in this gene, especially rs1344706, are thought to confer increased susceptibility to schizophrenia, bipolar disorder, and heroin addiciton. [provided by RefSeq, Nov 2015]
Known Variants94 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs10497655 | 2:185,462,041 | T/C | regulatory region variant | — |
| rs34714481 | 2:185,462,469 | A/G | regulatory region variant | — |
| rs359895 | 2:185,463,185 | T/A | regulatory region variant | — |
| rs149912547 | 2:185,463,700 | A/G | — | uncertain significance |
| rs1408646250 | 2:185,463,702 | A/T | — | uncertain significance |
| rs1296466900 | 2:185,463,717 | A/T | — | uncertain significance |
| rs7597593 | 2:185,533,580 | T/A | — | — |
| rs6723680 | 2:185,547,962 | A/G | intron variant | — |
| rs34481141 | 2:185,607,757 | A/G | intron variant | — |
| rs938277067 | 2:185,660,363 | G/T | — | — |
| rs2468380162 | 2:185,731,110 | G/T | — | uncertain significance |
| rs150769843 | 2:185,731,194 | G/A | — | benign |
| rs7603001 | 2:185,766,816 | A/T | — | — |
| rs1344706 | 2:185,778,428 | A/C | intron variant | — |
| rs4666998 | 2:185,780,221 | C/G | intron variant | — |
| rs13423388 | 2:185,780,225 | G/A | intron variant | — |
| rs56280129 | 2:185,780,306 | G/A | — | — |
| rs11681373 | 2:185,785,791 | A/G | intron variant | — |
| rs6755404 | 2:185,797,228 | A/T | — | — |
| rs115556450 | 2:185,798,445 | G/A | — | likely benign |
| rs144064575 | 2:185,800,556 | A/G | — | uncertain significance |
| rs367689479 | 2:185,800,640 | A/T | — | uncertain significance |
| rs943675787 | 2:185,800,653 | C/T | — | uncertain significance |
| rs201799996 | 2:185,800,655 | A/G | — | likely benign |
| rs370042078 | 2:185,800,722 | T/A | — | uncertain significance |
| rs148931756 | 2:185,800,792 | C/A | — | likely benign |
| rs762480136 | 2:185,800,853 | A/G | — | uncertain significance |
| rs748595144 | 2:185,800,893 | G/T | — | uncertain significance |
| rs12476147 | 2:185,800,905 | A/T | missense variant | benign |
| rs1415787156 | 2:185,800,971 | C/A | — | uncertain significance |
| rs138300291 | 2:185,800,995 | T/C | — | likely benign |
| rs762197994 | 2:185,801,018 | G/A | — | uncertain significance |
| rs373750240 | 2:185,801,024 | A/T | — | uncertain significance |
| rs139826553 | 2:185,801,097 | G/T | — | likely benign |
| rs2468469435 | 2:185,801,100 | A/T | — | uncertain significance |
| rs770127371 | 2:185,801,117 | G/C | — | uncertain significance |
| rs368984918 | 2:185,801,240 | C/A | — | uncertain significance |
| rs767729735 | 2:185,801,273 | G/A | — | uncertain significance |
| rs34345078 | 2:185,801,311 | C/T | — | likely benign |
| rs141114551 | 2:185,801,343 | T/A | — | likely benign |
| rs62198466 | 2:185,801,348 | A/G | — | likely benign |
| rs376585141 | 2:185,801,480 | A/G | — | uncertain significance |
| rs557343387 | 2:185,801,531 | A/G | — | uncertain significance |
| rs35676856 | 2:185,801,559 | A/G | — | benign |
| rs75132823 | 2:185,801,596 | C/T | — | benign |
| rs61739290 | 2:185,801,597 | A/G | — | benign |
| rs146785509 | 2:185,801,684 | A/T | — | likely benign |
| rs4667001 | 2:185,801,747 | G/A | — | benign |
| rs149183879 | 2:185,801,754 | C/T | — | uncertain significance |
| rs61739288 | 2:185,801,756 | G/A | — | benign |
| rs728534 | 2:185,801,917 | A/G | — | benign |
| rs144621375 | 2:185,801,937 | A/T | — | uncertain significance |
| rs2468471188 | 2:185,801,941 | T/A | — | uncertain significance |
| rs146611494 | 2:185,801,988 | C/G | — | conflicting classifications of pathogenicity |
| rs1685809106 | 2:185,802,088 | A/G | — | likely benign |
| rs139488901 | 2:185,802,089 | C/T | — | uncertain significance |
| rs771601434 | 2:185,802,154 | G/T | — | uncertain significance |
| rs1366842 | 2:185,802,243 | C/A | missense variant | benign |
| rs116133259 | 2:185,802,398 | A/G | — | benign |
| rs750195715 | 2:185,802,432 | G/A | — | uncertain significance |
| rs140191136 | 2:185,802,472 | A/C | — | uncertain significance |
| rs371359614 | 2:185,802,480 | A/G | — | uncertain significance |
| rs578257332 | 2:185,802,491 | C/T | — | likely benign |
| rs776630039 | 2:185,802,521 | A/G | — | uncertain significance |
| rs922627790 | 2:185,802,630 | T/C | — | uncertain significance |
| rs377532038 | 2:185,802,637 | C/A | — | uncertain significance |
| rs763354070 | 2:185,802,647 | T/G | — | uncertain significance |
| rs147519442 | 2:185,802,735 | A/G | — | uncertain significance |
| rs192749004 | 2:185,802,823 | G/A | — | uncertain significance |
| rs201469286 | 2:185,802,851 | G/A | — | likely benign |
| rs977438893 | 2:185,802,912 | A/G | — | uncertain significance |
| rs1465928740 | 2:185,802,935 | G/A | — | uncertain significance |
| rs780778290 | 2:185,803,009 | A/T | — | uncertain significance |
| rs150204094 | 2:185,803,132 | A/T | — | benign |
| rs1487864350 | 2:185,803,157 | G/C | — | uncertain significance |
| rs142034505 | 2:185,803,160 | A/T | — | likely benign |
| rs200513295 | 2:185,803,179 | C/A | — | uncertain significance |
| rs2468473896 | 2:185,803,252 | A/C | — | uncertain significance |
| rs190240911 | 2:185,803,307 | G/A | — | uncertain significance |
| rs991945944 | 2:185,803,340 | G/C | — | uncertain significance |
| rs141397832 | 2:185,803,352 | C/G | — | uncertain significance |
| rs3731834 | 2:185,803,364 | C/G | — | benign |
| rs2468474149 | 2:185,803,389 | C/G | — | uncertain significance |
| rs2468474176 | 2:185,803,413 | C/T | — | uncertain significance |
| rs193000214 | 2:185,803,442 | G/A | — | uncertain significance |
| rs112183442 | 2:185,803,445 | G/A | — | benign |
| rs201884581 | 2:185,803,472 | G/T | — | uncertain significance |
| rs138277674 | 2:185,803,480 | A/G | — | benign |
| rs754295294 | 2:185,803,508 | C/A | — | uncertain significance |
| rs141499616 | 2:185,803,582 | G/A | — | benign |
| rs762689676 | 2:185,803,605 | C/A | — | uncertain significance |
| rs767120954 | 2:185,803,649 | G/C | — | uncertain significance |
| rs2468474814 | 2:185,803,653 | T/G | — | uncertain significance |
| rs139802103 | 2:185,803,742 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.