ANKRD24
ankyrin repeat domain 24
Summary
Predicted to enable actin binding activity. Predicted to be involved in auditory receptor cell stereocilium organization and sensory perception of sound. Predicted to be located in plasma membrane. Predicted to be part of stereocilium. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants86 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1044243440 | 19:4,199,735 | T/C | — | uncertain significance |
| rs60004310 | 19:4,199,761 | C/T | — | uncertain significance |
| rs1055419943 | 19:4,199,762 | G/A | — | uncertain significance |
| rs368880588 | 19:4,199,957 | G/T | — | uncertain significance |
| rs373580986 | 19:4,199,969 | T/C | — | uncertain significance |
| rs781216347 | 19:4,200,106 | C/T | — | uncertain significance |
| rs374943322 | 19:4,200,111 | A/G | — | uncertain significance |
| rs769988640 | 19:4,202,875 | G/A | — | uncertain significance |
| rs199801260 | 19:4,207,293 | T/C | — | likely benign |
| rs757428983 | 19:4,207,308 | G/T | — | uncertain significance |
| rs372390380 | 19:4,207,504 | G/A | — | likely benign |
| rs2512501660 | 19:4,207,508 | C/T | — | uncertain significance |
| rs1161988078 | 19:4,207,598 | A/G | — | uncertain significance |
| rs769374619 | 19:4,207,903 | C/T | — | uncertain significance |
| rs200294304 | 19:4,207,957 | C/A | — | uncertain significance |
| rs760745612 | 19:4,208,775 | G/T | — | uncertain significance |
| rs762765184 | 19:4,208,784 | G/A | — | uncertain significance |
| rs111565354 | 19:4,209,424 | T/G | downstream gene variant | — |
| rs768886447 | 19:4,210,086 | C/T | — | uncertain significance |
| rs766705294 | 19:4,210,104 | C/T | — | uncertain significance |
| rs199656102 | 19:4,210,280 | G/A | — | uncertain significance |
| rs371351586 | 19:4,210,313 | C/T | — | uncertain significance |
| rs777701096 | 19:4,210,349 | A/G | — | uncertain significance |
| rs747333404 | 19:4,212,476 | C/T | — | uncertain significance |
| rs375444482 | 19:4,212,678 | C/T | — | uncertain significance |
| rs774411031 | 19:4,215,982 | G/A | — | uncertain significance |
| rs751053983 | 19:4,216,041 | C/T | — | likely benign |
| rs752310052 | 19:4,216,301 | A/G | — | uncertain significance |
| rs368327843 | 19:4,216,317 | C/T | — | uncertain significance |
| rs148030082 | 19:4,216,387 | G/A | — | uncertain significance |
| rs61742307 | 19:4,216,582 | G/T | — | uncertain significance |
| rs201346342 | 19:4,216,623 | A/G | — | uncertain significance |
| rs373345481 | 19:4,216,640 | G/A | — | uncertain significance |
| rs535707460 | 19:4,216,646 | G/A | — | uncertain significance |
| rs746780992 | 19:4,216,754 | G/A | — | uncertain significance |
| rs765439933 | 19:4,216,800 | G/T | — | uncertain significance |
| rs368093158 | 19:4,216,828 | C/T | — | likely benign |
| rs181048027 | 19:4,216,877 | G/T | — | uncertain significance |
| rs1206860676 | 19:4,216,884 | C/T | — | uncertain significance |
| rs377020129 | 19:4,216,902 | C/T | — | likely benign |
| rs773358130 | 19:4,216,929 | C/A | — | uncertain significance |
| rs202017923 | 19:4,217,001 | A/C | — | likely benign |
| rs749935492 | 19:4,217,004 | C/G | — | uncertain significance |
| rs367818983 | 19:4,217,006 | A/G | — | uncertain significance |
| rs61742138 | 19:4,217,058 | G/T | — | uncertain significance |
| rs776282831 | 19:4,217,071 | G/A | — | uncertain significance |
| rs201157676 | 19:4,217,096 | G/A | — | uncertain significance |
| rs376820525 | 19:4,217,105 | G/A | — | uncertain significance |
| rs200418117 | 19:4,217,123 | G/A | — | likely benign |
| rs1970147845 | 19:4,217,199 | G/A | — | uncertain significance |
| rs369990850 | 19:4,217,220 | G/C | — | uncertain significance |
| rs564768478 | 19:4,217,256 | C/T | — | likely benign |
| rs373357682 | 19:4,217,262 | C/T | — | uncertain significance |
| rs1324738491 | 19:4,217,315 | A/G | — | uncertain significance |
| rs1279765491 | 19:4,217,324 | G/A | — | uncertain significance |
| rs1970159974 | 19:4,217,325 | T/G | — | uncertain significance |
| rs778596061 | 19:4,217,366 | C/T | — | uncertain significance |
| rs973023270 | 19:4,217,372 | C/T | — | uncertain significance |
| rs765582446 | 19:4,217,451 | G/C | — | uncertain significance |
| rs150106684 | 19:4,217,576 | G/C | missense variant | — |
| rs1970187951 | 19:4,217,645 | C/T | — | uncertain significance |
| rs1160871466 | 19:4,217,648 | G/C | — | uncertain significance |
| rs2512560576 | 19:4,217,657 | G/A | — | uncertain significance |
| rs1428767451 | 19:4,217,687 | C/G | — | uncertain significance |
| rs1001173672 | 19:4,217,733 | C/T | — | uncertain significance |
| rs199645648 | 19:4,217,763 | C/T | — | uncertain significance |
| rs1313360465 | 19:4,217,807 | C/G | — | uncertain significance |
| rs1299828769 | 19:4,217,858 | G/A | — | uncertain significance |
| rs760143910 | 19:4,217,931 | A/C | — | uncertain significance |
| rs571444889 | 19:4,217,945 | C/T | — | uncertain significance |
| rs1268125908 | 19:4,217,979 | T/G | — | uncertain significance |
| rs376111459 | 19:4,218,138 | A/C | — | uncertain significance |
| rs1252391468 | 19:4,218,141 | C/T | — | uncertain significance |
| rs1193578267 | 19:4,218,145 | C/A | — | uncertain significance |
| rs1195801120 | 19:4,218,146 | G/T | — | uncertain significance |
| rs767243018 | 19:4,219,616 | G/C | — | uncertain significance |
| rs764871323 | 19:4,219,633 | G/A | — | uncertain significance |
| rs755420735 | 19:4,219,654 | G/C | — | uncertain significance |
| rs749955664 | 19:4,219,697 | G/T | — | uncertain significance |
| rs762688279 | 19:4,219,703 | C/T | — | uncertain significance |
| rs370271902 | 19:4,222,742 | G/A | — | uncertain significance |
| rs766500514 | 19:4,224,131 | C/T | — | uncertain significance |
| rs192375344 | 19:4,224,147 | C/T | — | likely benign |
| rs367894541 | 19:4,224,148 | G/A | — | uncertain significance |
| rs377369259 | 19:4,224,497 | C/T | — | uncertain significance |
| rs371340481 | 19:4,224,498 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.