ANKRD28
ankyrin repeat domain 28
Summary
Predicted to be located in cytosol and nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants69 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1575055984 | 3:15,711,790 | G/C | — | uncertain significance |
| rs2471617380 | 3:15,711,848 | T/A | — | uncertain significance |
| rs368821167 | 3:15,711,889 | A/G | — | uncertain significance |
| rs372742448 | 3:15,711,895 | A/G | — | uncertain significance |
| rs761298767 | 3:15,718,491 | C/A | — | uncertain significance |
| rs149481554 | 3:15,718,494 | C/T | — | uncertain significance |
| rs2067005440 | 3:15,718,517 | C/T | — | uncertain significance |
| rs762717215 | 3:15,719,020 | A/T | — | uncertain significance |
| rs759882787 | 3:15,719,047 | A/C | — | uncertain significance |
| rs754766441 | 3:15,719,784 | T/C | — | uncertain significance |
| rs752589114 | 3:15,719,790 | T/G | — | uncertain significance |
| rs369691636 | 3:15,719,818 | A/G | — | likely benign |
| rs779746458 | 3:15,720,812 | C/T | — | uncertain significance |
| rs1302708063 | 3:15,720,821 | C/T | — | uncertain significance |
| rs369791320 | 3:15,720,880 | T/C | — | uncertain significance |
| rs776255831 | 3:15,721,013 | C/T | — | uncertain significance |
| rs199920401 | 3:15,726,735 | T/C | — | uncertain significance |
| rs2067985847 | 3:15,726,822 | G/C | — | uncertain significance |
| rs773032840 | 3:15,726,837 | A/G | — | uncertain significance |
| rs370032840 | 3:15,726,888 | C/T | — | uncertain significance |
| rs372790335 | 3:15,726,898 | A/C | — | uncertain significance |
| rs548976081 | 3:15,726,911 | T/G | — | uncertain significance |
| rs774546032 | 3:15,727,789 | C/T | — | uncertain significance |
| rs201138281 | 3:15,731,571 | A/C | — | uncertain significance |
| rs373074737 | 3:15,731,691 | C/G | — | uncertain significance |
| rs370968562 | 3:15,736,271 | G/C | — | uncertain significance |
| rs1332966114 | 3:15,737,642 | A/G | — | uncertain significance |
| rs369238834 | 3:15,737,676 | A/C | — | uncertain significance |
| rs757361546 | 3:15,737,708 | C/A | — | uncertain significance |
| rs2472280196 | 3:15,737,712 | T/A | — | uncertain significance |
| rs2472280287 | 3:15,737,714 | C/T | — | uncertain significance |
| rs2276752 | 3:15,749,555 | C/T | — | uncertain significance |
| rs750271173 | 3:15,751,218 | G/C | — | uncertain significance |
| rs373054566 | 3:15,753,649 | G/A | — | uncertain significance |
| rs746296012 | 3:15,753,695 | C/A | — | uncertain significance |
| rs201348489 | 3:15,755,044 | C/T | — | uncertain significance |
| rs541101742 | 3:15,755,091 | C/T | — | uncertain significance |
| rs201242217 | 3:15,755,098 | C/T | — | uncertain significance |
| rs372312590 | 3:15,762,444 | T/A | — | uncertain significance |
| rs747339688 | 3:15,762,505 | G/A | — | uncertain significance |
| rs373009412 | 3:15,762,513 | C/T | — | uncertain significance |
| rs201631150 | 3:15,762,552 | A/G | — | uncertain significance |
| rs2472977864 | 3:15,762,582 | T/C | — | uncertain significance |
| rs565056573 | 3:15,762,625 | G/A | — | uncertain significance |
| rs200316353 | 3:15,765,941 | G/A | — | uncertain significance |
| rs552527501 | 3:15,766,001 | G/A | — | uncertain significance |
| rs13079440 | 3:15,769,094 | A/C | — | — |
| rs2074953865 | 3:15,776,986 | A/G | — | uncertain significance |
| rs886818290 | 3:15,778,589 | C/T | — | uncertain significance |
| rs2075070182 | 3:15,778,624 | C/G | — | uncertain significance |
| rs567905985 | 3:15,778,655 | G/C | — | uncertain significance |
| rs1335039910 | 3:15,778,725 | G/C | — | uncertain significance |
| rs1266104445 | 3:15,778,730 | T/C | — | uncertain significance |
| rs2455850 | 3:15,782,711 | A/C | downstream gene variant | — |
| rs6442546 | 3:15,789,996 | C/G | — | — |
| rs13069238 | 3:15,790,775 | G/C | — | — |
| rs781415601 | 3:15,807,750 | T/G | — | uncertain significance |
| rs138689821 | 3:15,807,793 | G/A | — | likely benign |
| rs760104686 | 3:15,807,806 | C/T | — | uncertain significance |
| rs553679983 | 3:15,821,554 | C/T | — | — |
| rs2345736 | 3:15,824,860 | T/A | — | — |
| rs1584324 | 3:15,833,653 | C/T | intron variant | — |
| rs761297821 | 3:15,836,795 | T/C | — | uncertain significance |
| rs4685262 | 3:15,853,661 | C/A | intron variant | — |
| rs6807029 | 3:15,869,857 | A/T | — | — |
| rs1052392273 | 3:15,870,669 | C/T | — | — |
| rs13075529 | 3:15,870,752 | T/A | intron variant | — |
| rs11128761 | 3:15,874,482 | C/T | intron variant | — |
| rs6773547 | 3:15,882,245 | C/T | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.