ZNF609
zinc finger protein 609
Summary
Predicted to enable promoter-specific chromatin binding activity. Involved in regulation of myoblast proliferation. Located in nucleoplasm. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants83 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs565496052 | 15:64,791,664 | A/C | — | uncertain significance |
| rs1893528224 | 15:64,791,680 | A/G | — | uncertain significance |
| rs750522477 | 15:64,791,739 | G/A | — | uncertain significance |
| rs777189733 | 15:64,791,892 | A/G | — | uncertain significance |
| rs375242172 | 15:64,791,896 | G/A | — | likely benign |
| rs767713276 | 15:64,791,953 | G/C | — | uncertain significance |
| rs756586641 | 15:64,792,007 | A/G | — | uncertain significance |
| rs151216141 | 15:64,792,042 | G/T | — | benign |
| rs372616335 | 15:64,792,055 | C/T | — | uncertain significance |
| rs543917172 | 15:64,792,081 | G/A | — | uncertain significance |
| rs367960309 | 15:64,792,333 | T/C | — | uncertain significance |
| rs374998036 | 15:64,792,336 | C/T | — | uncertain significance |
| rs754415983 | 15:64,792,358 | C/T | — | uncertain significance |
| rs202183286 | 15:64,880,644 | G/T | — | — |
| rs749480910 | 15:64,915,045 | C/T | — | uncertain significance |
| rs753507083 | 15:64,915,087 | A/T | — | uncertain significance |
| rs771940316 | 15:64,915,138 | T/C | — | uncertain significance |
| rs145531900 | 15:64,915,146 | A/G | — | uncertain significance |
| rs749937430 | 15:64,966,315 | C/T | — | uncertain significance |
| rs779545164 | 15:64,966,317 | C/A | — | uncertain significance |
| rs2505863798 | 15:64,966,345 | A/G | — | uncertain significance |
| rs772149162 | 15:64,966,395 | A/G | — | uncertain significance |
| rs200890644 | 15:64,966,530 | G/A | — | uncertain significance |
| rs774366281 | 15:64,966,762 | G/A | — | uncertain significance |
| rs771573878 | 15:64,966,767 | G/A | — | uncertain significance |
| rs1190113400 | 15:64,966,791 | T/A | — | uncertain significance |
| rs2141015050 | 15:64,966,872 | G/T | — | uncertain significance |
| rs2505864754 | 15:64,966,875 | G/A | — | uncertain significance |
| rs775025779 | 15:64,966,915 | A/G | — | uncertain significance |
| rs201678172 | 15:64,966,921 | C/G | — | uncertain significance |
| rs147230020 | 15:64,966,927 | A/G | — | uncertain significance |
| rs774578999 | 15:64,966,935 | G/C | — | uncertain significance |
| rs778825538 | 15:64,967,022 | C/T | — | uncertain significance |
| rs745636514 | 15:64,967,023 | G/A | — | uncertain significance |
| rs779995888 | 15:64,967,035 | C/T | — | uncertain significance |
| rs370988343 | 15:64,967,047 | C/A | — | uncertain significance |
| rs370787772 | 15:64,967,185 | T/C | — | uncertain significance |
| rs1240984132 | 15:64,967,334 | A/G | — | uncertain significance |
| rs770273665 | 15:64,967,398 | A/G | — | uncertain significance |
| rs773329924 | 15:64,967,404 | G/T | — | uncertain significance |
| rs2505865977 | 15:64,967,415 | A/G | — | uncertain significance |
| rs764781414 | 15:64,967,473 | T/C | — | uncertain significance |
| rs148104351 | 15:64,967,502 | A/G | — | uncertain significance |
| rs761775154 | 15:64,967,539 | C/G | — | uncertain significance |
| rs751135506 | 15:64,967,575 | A/G | — | uncertain significance |
| rs2505866485 | 15:64,967,631 | G/T | — | uncertain significance |
| rs1412609410 | 15:64,967,817 | C/G | — | uncertain significance |
| rs1343136188 | 15:64,967,856 | A/G | — | uncertain significance |
| rs2505867024 | 15:64,967,859 | G/A | — | uncertain significance |
| rs149658249 | 15:64,967,878 | A/G | — | uncertain significance |
| rs773888080 | 15:64,967,889 | G/C | — | uncertain significance |
| rs756288284 | 15:64,967,952 | A/G | — | uncertain significance |
| rs1371495228 | 15:64,967,966 | C/G | — | likely benign |
| rs373154384 | 15:64,967,998 | C/A | — | uncertain significance |
| rs370146037 | 15:64,968,049 | C/T | — | uncertain significance |
| rs199759765 | 15:64,968,085 | G/A | — | uncertain significance |
| rs201362987 | 15:64,968,108 | C/T | — | uncertain significance |
| rs780688751 | 15:64,968,207 | A/G | — | uncertain significance |
| rs116277489 | 15:64,968,272 | C/T | — | benign |
| rs369238345 | 15:64,968,298 | A/C | — | uncertain significance |
| rs918339043 | 15:64,968,333 | C/T | — | uncertain significance |
| rs766155667 | 15:64,968,402 | G/A | — | uncertain significance |
| rs749359068 | 15:64,970,368 | C/G | — | uncertain significance |
| rs537647542 | 15:64,970,372 | T/G | — | uncertain significance |
| rs138145515 | 15:64,970,429 | C/T | — | uncertain significance |
| rs555512820 | 15:64,970,480 | G/A | — | uncertain significance |
| rs769413393 | 15:64,970,532 | G/A | — | uncertain significance |
| rs143601788 | 15:64,970,535 | C/G | — | uncertain significance |
| rs141348798 | 15:64,970,594 | A/G | — | uncertain significance |
| rs765691880 | 15:64,970,646 | G/A | — | uncertain significance |
| rs200173822 | 15:64,972,391 | C/T | — | benign |
| rs373108405 | 15:64,972,558 | C/T | — | uncertain significance |
| rs2505874455 | 15:64,972,897 | G/A | — | uncertain significance |
| rs373171885 | 15:64,972,920 | G/A | — | uncertain significance |
| rs139876697 | 15:64,972,935 | G/A | — | uncertain significance |
| rs776853566 | 15:64,972,939 | G/T | — | uncertain significance |
| rs1346322934 | 15:64,972,950 | G/A | — | uncertain significance |
| rs751411151 | 15:64,972,962 | C/T | — | uncertain significance |
| rs1595762985 | 15:64,972,965 | A/G | — | uncertain significance |
| rs8028030 | 15:64,972,967 | C/T | — | benign |
| rs1381024670 | 15:64,972,980 | C/T | — | uncertain significance |
| rs2505874785 | 15:64,973,007 | C/T | — | uncertain significance |
| rs151125949 | 15:64,973,044 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.