ANKRD55
ankyrin repeat domain 55
Known Variants61 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs3930044 | 5:55,395,610 | G/T | regulatory region variant | — |
| rs144419437 | 5:55,396,022 | A/T | — | uncertain significance |
| rs766207133 | 5:55,396,110 | C/T | — | uncertain significance |
| rs751625585 | 5:55,398,322 | T/A | — | uncertain significance |
| rs757935376 | 5:55,398,357 | T/C | — | uncertain significance |
| rs143266332 | 5:55,406,990 | C/A | — | uncertain significance |
| rs2533852343 | 5:55,406,993 | C/G | — | uncertain significance |
| rs2533852544 | 5:55,407,046 | G/A | — | uncertain significance |
| rs778736276 | 5:55,407,154 | C/A | — | uncertain significance |
| rs778032307 | 5:55,407,176 | C/T | — | uncertain significance |
| rs2533853142 | 5:55,407,191 | C/G | — | uncertain significance |
| rs143094717 | 5:55,407,268 | C/T | — | uncertain significance |
| rs770473679 | 5:55,407,274 | G/A | — | uncertain significance |
| rs150293961 | 5:55,407,281 | T/C | — | uncertain significance |
| rs772756747 | 5:55,407,299 | G/A | — | uncertain significance |
| rs2533853706 | 5:55,407,341 | C/T | — | uncertain significance |
| rs369403534 | 5:55,407,380 | C/T | — | uncertain significance |
| rs77017041 | 5:55,407,449 | A/G | — | likely benign |
| rs759075872 | 5:55,407,469 | C/T | — | likely benign |
| rs143919551 | 5:55,407,497 | C/T | — | uncertain significance |
| rs76363118 | 5:55,407,523 | C/T | — | likely benign |
| rs1303936481 | 5:55,407,527 | A/G | — | uncertain significance |
| rs551715515 | 5:55,407,533 | G/C | — | uncertain significance |
| rs1438364927 | 5:55,407,575 | T/C | — | uncertain significance |
| rs2533864675 | 5:55,412,449 | C/T | — | uncertain significance |
| rs186718700 | 5:55,412,476 | T/C | — | uncertain significance |
| rs569831356 | 5:55,412,496 | T/C | — | uncertain significance |
| rs1228528929 | 5:55,412,548 | A/C | — | uncertain significance |
| rs983787813 | 5:55,412,569 | A/C | — | uncertain significance |
| rs146546015 | 5:55,412,572 | C/T | — | likely benign |
| rs415407 | 5:55,414,956 | A/T | — | — |
| rs115312705 | 5:55,422,688 | T/G | regulatory region variant | — |
| rs575822491 | 5:55,422,806 | A/G | — | uncertain significance |
| rs61741176 | 5:55,422,823 | C/T | — | benign |
| rs372499783 | 5:55,422,879 | T/A | — | uncertain significance |
| rs773608846 | 5:55,422,887 | C/G | — | uncertain significance |
| rs62363956 | 5:55,426,163 | C/A | — | — |
| rs6873385 | 5:55,436,851 | T/A | downstream gene variant | — |
| rs6859219 | 5:55,438,580 | C/A | regulatory region variant | — |
| rs10065637 | 5:55,438,851 | C/T | regulatory region variant | — |
| rs746434017 | 5:55,439,668 | A/G | — | uncertain significance |
| rs780505029 | 5:55,439,672 | G/A | — | uncertain significance |
| rs71624119 | 5:55,440,730 | G/C | — | — |
| rs7731626 | 5:55,444,683 | G/C | — | — |
| rs10077826 | 5:55,450,211 | C/T | intron variant | — |
| rs28722705 | 5:55,453,942 | A/T | intron variant | — |
| rs2478243087 | 5:55,455,665 | T/C | — | uncertain significance |
| rs1580990955 | 5:55,455,669 | C/T | — | likely benign |
| rs574664631 | 5:55,466,528 | C/T | — | uncertain significance |
| rs773050862 | 5:55,466,561 | G/A | — | uncertain significance |
| rs771155798 | 5:55,466,566 | T/C | — | uncertain significance |
| rs2478276897 | 5:55,471,995 | C/T | — | uncertain significance |
| rs149513316 | 5:55,472,055 | A/G | — | uncertain significance |
| rs148696905 | 5:55,472,077 | G/A | — | uncertain significance |
| rs1192765657 | 5:55,479,431 | A/G | — | uncertain significance |
| rs4700060 | 5:55,510,656 | C/T | intron variant | — |
| rs764391102 | 5:55,528,714 | G/T | — | uncertain significance |
| rs1760294315 | 5:55,528,717 | A/T | — | uncertain significance |
| rs1386005065 | 5:55,528,718 | T/A | — | uncertain significance |
| rs1017306668 | 5:55,528,721 | A/C | — | uncertain significance |
| rs8180499 | 5:55,530,306 | A/G | upstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.