ANKDD1A
ankyrin repeat and death domain containing 1A
Summary
Predicted to be involved in signal transduction. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants44 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1306407172 | 15:65,204,146 | C/A | — | uncertain significance |
| rs2506041214 | 15:65,204,160 | G/A | — | uncertain significance |
| rs370256531 | 15:65,208,065 | T/C | — | uncertain significance |
| rs999839839 | 15:65,209,672 | G/A | — | uncertain significance |
| rs369578168 | 15:65,209,691 | C/T | — | uncertain significance |
| rs200840260 | 15:65,214,122 | T/G | — | uncertain significance |
| rs145919740 | 15:65,214,133 | C/T | — | uncertain significance |
| rs1348511888 | 15:65,214,136 | T/C | — | uncertain significance |
| rs201916280 | 15:65,214,166 | G/A | — | likely benign |
| rs774900398 | 15:65,214,192 | G/C | — | uncertain significance |
| rs759977930 | 15:65,214,195 | G/A | — | uncertain significance |
| rs2506049539 | 15:65,218,324 | C/A | — | uncertain significance |
| rs1388281354 | 15:65,218,340 | G/A | — | uncertain significance |
| rs761588607 | 15:65,219,113 | C/T | — | uncertain significance |
| rs765982673 | 15:65,219,135 | C/G | — | uncertain significance |
| rs140781481 | 15:65,223,078 | G/A | — | uncertain significance |
| rs778435913 | 15:65,223,107 | G/A | — | uncertain significance |
| rs745367546 | 15:65,223,108 | A/T | — | uncertain significance |
| rs2506052593 | 15:65,223,695 | C/T | — | uncertain significance |
| rs140684706 | 15:65,223,728 | C/G | — | uncertain significance |
| rs769128553 | 15:65,226,371 | T/G | — | uncertain significance |
| rs148267097 | 15:65,226,376 | C/T | — | uncertain significance |
| rs537030205 | 15:65,226,390 | C/T | — | uncertain significance |
| rs138584260 | 15:65,226,396 | C/G | — | uncertain significance |
| rs755542121 | 15:65,226,405 | G/A | — | uncertain significance |
| rs756222100 | 15:65,226,417 | G/T | — | uncertain significance |
| rs377389557 | 15:65,234,711 | C/T | — | likely benign |
| rs765833491 | 15:65,235,698 | C/T | — | uncertain significance |
| rs1156678774 | 15:65,235,730 | A/G | — | uncertain significance |
| rs922734417 | 15:65,235,738 | T/C | — | uncertain significance |
| rs141438800 | 15:65,236,889 | A/G | — | uncertain significance |
| rs1312867124 | 15:65,236,909 | A/C | — | uncertain significance |
| rs1465711414 | 15:65,236,925 | G/A | — | uncertain significance |
| rs561180507 | 15:65,239,640 | C/G | — | uncertain significance |
| rs1167667376 | 15:65,239,675 | C/T | — | uncertain significance |
| rs1030713804 | 15:65,239,702 | G/A | — | uncertain significance |
| rs571389209 | 15:65,239,703 | T/C | — | uncertain significance |
| rs201425371 | 15:65,239,712 | G/A | — | likely benign |
| rs760119932 | 15:65,239,775 | C/T | — | uncertain significance |
| rs777612217 | 15:65,239,798 | G/A | — | uncertain significance |
| rs138418526 | 15:65,242,157 | G/A | — | uncertain significance |
| rs748011284 | 15:65,242,163 | C/T | — | uncertain significance |
| rs200697715 | 15:65,242,165 | C/T | — | likely benign |
| rs1429505814 | 15:65,242,172 | A/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.