ANKRD52
ankyrin repeat domain 52
Known Variants38 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs72648137 | 12:56,634,827 | A/G | — | — |
| rs760776825 | 12:56,636,958 | C/T | — | uncertain significance |
| rs2547145537 | 12:56,636,978 | T/A | — | uncertain significance |
| rs769320051 | 12:56,637,009 | C/T | — | uncertain significance |
| rs773443613 | 12:56,637,030 | C/T | — | uncertain significance |
| rs372191802 | 12:56,637,035 | G/A | — | uncertain significance |
| rs748731346 | 12:56,637,146 | T/C | — | uncertain significance |
| rs369865039 | 12:56,637,640 | C/T | — | uncertain significance |
| rs752076387 | 12:56,637,859 | T/C | — | uncertain significance |
| rs776466027 | 12:56,638,162 | G/A | — | uncertain significance |
| rs764716428 | 12:56,638,180 | A/G | — | uncertain significance |
| rs2547147038 | 12:56,638,470 | C/T | — | uncertain significance |
| rs201659742 | 12:56,638,483 | C/T | — | uncertain significance |
| rs766786981 | 12:56,638,502 | C/T | — | uncertain significance |
| rs777966459 | 12:56,638,535 | G/A | — | uncertain significance |
| rs748863721 | 12:56,638,574 | G/A | — | uncertain significance |
| rs199849831 | 12:56,638,942 | G/T | — | uncertain significance |
| rs148806264 | 12:56,638,971 | T/C | — | uncertain significance |
| rs1489734027 | 12:56,639,302 | G/A | — | uncertain significance |
| rs2547148976 | 12:56,641,504 | G/A | — | uncertain significance |
| rs777085738 | 12:56,641,903 | G/A | — | uncertain significance |
| rs755939369 | 12:56,641,954 | G/C | — | uncertain significance |
| rs201137450 | 12:56,642,341 | T/C | — | uncertain significance |
| rs774217421 | 12:56,645,818 | G/A | — | uncertain significance |
| rs189462588 | 12:56,645,871 | G/A | — | uncertain significance |
| rs1244186415 | 12:56,645,978 | C/T | — | uncertain significance |
| rs527280209 | 12:56,645,984 | C/T | — | uncertain significance |
| rs111320403 | 12:56,646,072 | G/A | — | benign |
| rs200980927 | 12:56,646,651 | C/A | — | uncertain significance |
| rs2547152378 | 12:56,646,678 | T/C | — | uncertain significance |
| rs1293583016 | 12:56,647,177 | A/G | — | uncertain significance |
| rs202238056 | 12:56,648,021 | C/T | — | uncertain significance |
| rs115543175 | 12:56,648,066 | G/A | — | benign |
| rs200485121 | 12:56,648,366 | G/A | — | uncertain significance |
| rs376052315 | 12:56,651,073 | T/A | — | uncertain significance |
| rs79310796 | 12:56,651,618 | A/T | — | uncertain significance |
| rs1258360435 | 12:56,652,032 | C/G | — | uncertain significance |
| rs61937678 | 12:56,653,695 | T/A | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.