ANKMY1
ankyrin repeat and MYND domain containing 1
Summary
Predicted to enable zinc ion binding activity. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants90 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2529100866 | 2:241,419,055 | C/T | — | uncertain significance |
| rs1248633789 | 2:241,419,067 | G/T | — | uncertain significance |
| rs147804085 | 2:241,420,373 | G/A | — | likely benign |
| rs149189286 | 2:241,420,438 | C/T | — | uncertain significance |
| rs767852164 | 2:241,420,449 | G/A | — | uncertain significance |
| rs574952192 | 2:241,420,465 | G/A | — | uncertain significance |
| rs748134301 | 2:241,420,479 | C/G | — | uncertain significance |
| rs777298013 | 2:241,421,678 | G/A | — | likely benign |
| rs186776971 | 2:241,435,232 | C/T | intron variant | — |
| rs573972313 | 2:241,435,256 | A/G | — | — |
| rs560711091 | 2:241,435,894 | T/C | — | — |
| rs149855626 | 2:241,439,437 | C/T | — | uncertain significance |
| rs766289505 | 2:241,439,468 | G/A | — | uncertain significance |
| rs141314665 | 2:241,439,473 | C/T | — | uncertain significance |
| rs369197129 | 2:241,439,492 | G/A | — | uncertain significance |
| rs772241901 | 2:241,439,502 | C/T | — | uncertain significance |
| rs201792868 | 2:241,439,891 | T/C | — | uncertain significance |
| rs745738810 | 2:241,439,892 | A/C | — | uncertain significance |
| rs147582329 | 2:241,439,955 | C/T | — | uncertain significance |
| rs140796181 | 2:241,439,956 | G/A | — | benign |
| rs553748723 | 2:241,446,997 | T/C | — | likely benign |
| rs2530884164 | 2:241,447,035 | C/T | — | uncertain significance |
| rs779037689 | 2:241,447,108 | C/T | — | likely benign |
| rs748999358 | 2:241,448,784 | A/G | — | uncertain significance |
| rs147534670 | 2:241,448,808 | C/T | — | uncertain significance |
| rs377459989 | 2:241,448,836 | C/T | — | likely benign |
| rs570625017 | 2:241,448,853 | C/T | — | likely benign |
| rs771425474 | 2:241,448,856 | A/G | — | uncertain significance |
| rs370283686 | 2:241,451,298 | C/T | — | uncertain significance |
| rs779402768 | 2:241,451,329 | C/G | — | uncertain significance |
| rs759583163 | 2:241,451,336 | G/A | — | uncertain significance |
| rs377526714 | 2:241,451,364 | C/G | — | uncertain significance |
| rs142973511 | 2:241,451,367 | G/C | — | uncertain significance |
| rs369562071 | 2:241,452,223 | C/A | — | uncertain significance |
| rs770466778 | 2:241,452,260 | C/T | — | uncertain significance |
| rs201506288 | 2:241,452,299 | T/G | — | uncertain significance |
| rs370594143 | 2:241,452,308 | C/T | — | uncertain significance |
| rs762476674 | 2:241,452,352 | G/A | — | uncertain significance |
| rs114285255 | 2:241,457,727 | G/A | intron variant | — |
| rs373381211 | 2:241,459,787 | G/T | — | uncertain significance |
| rs759696893 | 2:241,459,811 | C/G | — | uncertain significance |
| rs376796882 | 2:241,459,841 | C/T | — | uncertain significance |
| rs753533005 | 2:241,459,913 | G/A | — | uncertain significance |
| rs775175409 | 2:241,463,303 | C/T | — | uncertain significance |
| rs140290900 | 2:241,463,327 | G/A | — | uncertain significance |
| rs760017246 | 2:241,463,360 | G/A | — | uncertain significance |
| rs141510821 | 2:241,463,399 | C/A | — | uncertain significance |
| rs184584055 | 2:241,463,422 | G/A | — | uncertain significance |
| rs764591424 | 2:241,463,441 | C/T | — | likely benign |
| rs201824658 | 2:241,463,470 | G/A | — | uncertain significance |
| rs767655569 | 2:241,463,501 | T/C | — | uncertain significance |
| rs747966097 | 2:241,463,525 | C/T | — | uncertain significance |
| rs149945594 | 2:241,463,544 | G/C | — | uncertain significance |
| rs769318304 | 2:241,463,561 | G/C | — | uncertain significance |
| rs2082890844 | 2:241,463,609 | A/G | — | uncertain significance |
| rs376438301 | 2:241,463,654 | C/T | — | likely benign |
| rs145705338 | 2:241,463,655 | G/A | — | benign |
| rs763738953 | 2:241,463,671 | G/T | — | likely benign |
| rs149263381 | 2:241,463,758 | G/A | — | uncertain significance |
| rs756484662 | 2:241,465,133 | T/C | — | uncertain significance |
| rs267599283 | 2:241,465,145 | G/A | — | uncertain significance |
| rs199589162 | 2:241,465,152 | C/T | — | uncertain significance |
| rs374902226 | 2:241,465,187 | G/A | — | uncertain significance |
| rs1282345357 | 2:241,465,256 | T/C | — | uncertain significance |
| rs192708554 | 2:241,465,785 | G/A | — | uncertain significance |
| rs140025275 | 2:241,465,797 | G/A | — | uncertain significance |
| rs1297462340 | 2:241,468,493 | G/C | — | uncertain significance |
| rs967184823 | 2:241,468,526 | T/A | — | uncertain significance |
| rs776862271 | 2:241,468,562 | C/T | — | uncertain significance |
| rs374795351 | 2:241,468,571 | A/G | — | uncertain significance |
| rs72998048 | 2:241,468,605 | G/T | — | likely benign |
| rs750079817 | 2:241,468,631 | A/G | — | likely benign |
| rs371764320 | 2:241,468,652 | T/C | — | uncertain significance |
| rs148669449 | 2:241,468,662 | G/T | — | uncertain significance |
| rs765852536 | 2:241,468,694 | T/A | — | uncertain significance |
| rs150525285 | 2:241,468,750 | G/T | — | benign |
| rs74001686 | 2:241,468,772 | C/G | — | benign |
| rs933998332 | 2:241,468,781 | T/C | — | uncertain significance |
| rs201536200 | 2:241,468,887 | C/T | — | uncertain significance |
| rs1025855426 | 2:241,468,892 | C/T | — | uncertain significance |
| rs746311436 | 2:241,492,357 | T/C | — | uncertain significance |
| rs768966375 | 2:241,492,374 | C/T | — | uncertain significance |
| rs759373344 | 2:241,492,398 | G/A | — | uncertain significance |
| rs752343809 | 2:241,492,418 | C/A | — | uncertain significance |
| rs1211896947 | 2:241,492,422 | A/C | — | uncertain significance |
| rs2535489274 | 2:241,494,290 | G/A | — | uncertain significance |
| rs375514209 | 2:241,494,301 | G/C | — | uncertain significance |
| rs367784859 | 2:241,494,332 | C/A | — | uncertain significance |
| rs2092118347 | 2:241,494,344 | T/C | — | likely benign |
| rs4305276 | 2:241,495,013 | C/T | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.