ANKS3
ankyrin repeat and sterile alpha motif domain containing 3
Summary
Predicted to be located in cytoplasm. Predicted to be active in cilium. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants77 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2306769 | 16:4,746,783 | G/T | downstream gene variant | — |
| rs1475680585 | 16:4,747,073 | C/T | — | uncertain significance |
| rs771922471 | 16:4,747,342 | C/T | — | likely benign |
| rs182756690 | 16:4,747,348 | C/T | — | uncertain significance |
| rs759934558 | 16:4,747,367 | A/C | — | uncertain significance |
| rs781408628 | 16:4,747,385 | T/C | — | uncertain significance |
| rs2079622654 | 16:4,747,394 | G/T | — | uncertain significance |
| rs146041043 | 16:4,747,407 | G/A | — | likely benign |
| rs769008777 | 16:4,747,987 | G/A | — | uncertain significance |
| rs139954601 | 16:4,747,990 | C/T | — | uncertain significance |
| rs529727002 | 16:4,747,998 | C/T | — | uncertain significance |
| rs370919758 | 16:4,748,019 | G/A | — | uncertain significance |
| rs34901190 | 16:4,748,033 | C/G | — | benign |
| rs148408215 | 16:4,748,043 | G/A | — | likely benign |
| rs773992282 | 16:4,748,052 | G/C | — | uncertain significance |
| rs1046449584 | 16:4,748,461 | G/A | — | uncertain significance |
| rs2079702970 | 16:4,748,465 | G/C | — | uncertain significance |
| rs762828564 | 16:4,748,501 | C/T | — | likely benign |
| rs761207585 | 16:4,748,507 | C/T | — | uncertain significance |
| rs377174585 | 16:4,748,578 | G/A | — | likely benign |
| rs755623227 | 16:4,748,594 | C/T | — | uncertain significance |
| rs745649922 | 16:4,748,600 | G/A | — | uncertain significance |
| rs889913932 | 16:4,748,818 | C/T | — | uncertain significance |
| rs2079739501 | 16:4,748,865 | A/G | — | uncertain significance |
| rs756410421 | 16:4,748,916 | G/A | — | uncertain significance |
| rs377633164 | 16:4,749,112 | G/C | — | uncertain significance |
| rs2506919795 | 16:4,749,141 | T/C | — | uncertain significance |
| rs775915015 | 16:4,749,170 | G/A | — | uncertain significance |
| rs2506952520 | 16:4,750,975 | G/A | — | uncertain significance |
| rs556840530 | 16:4,751,011 | G/T | — | uncertain significance |
| rs369241127 | 16:4,751,023 | A/G | — | uncertain significance |
| rs144928887 | 16:4,751,025 | G/A | — | likely benign |
| rs149148220 | 16:4,751,047 | C/T | — | uncertain significance |
| rs145685232 | 16:4,751,105 | G/A | — | uncertain significance |
| rs2506955773 | 16:4,751,114 | T/A | — | uncertain significance |
| rs61747669 | 16:4,751,124 | A/G | — | benign |
| rs370067651 | 16:4,751,437 | C/T | — | uncertain significance |
| rs141717553 | 16:4,751,439 | T/C | — | uncertain significance |
| rs755972798 | 16:4,751,505 | C/T | — | uncertain significance |
| rs138068446 | 16:4,751,514 | G/A | — | uncertain significance |
| rs184951481 | 16:4,751,550 | G/A | — | likely benign |
| rs76733899 | 16:4,752,128 | C/T | — | benign |
| rs142774375 | 16:4,752,177 | C/T | — | uncertain significance |
| rs1314380338 | 16:4,752,193 | G/T | — | uncertain significance |
| rs200063628 | 16:4,752,199 | C/T | — | uncertain significance |
| rs757755400 | 16:4,752,201 | C/G | — | uncertain significance |
| rs779197274 | 16:4,752,204 | C/T | — | uncertain significance |
| rs749232019 | 16:4,752,232 | G/A | — | uncertain significance |
| rs373599022 | 16:4,755,101 | C/T | — | uncertain significance |
| rs765677118 | 16:4,755,107 | C/T | — | likely benign |
| rs78074706 | 16:4,755,108 | G/A | missense variant | — |
| rs755830521 | 16:4,755,120 | C/T | — | uncertain significance |
| rs758439656 | 16:4,755,166 | G/C | — | uncertain significance |
| rs1313638596 | 16:4,755,173 | C/T | — | uncertain significance |
| rs201941428 | 16:4,755,179 | C/G | — | uncertain significance |
| rs201554424 | 16:4,755,206 | T/C | — | uncertain significance |
| rs142015202 | 16:4,755,246 | C/T | — | uncertain significance |
| rs149773834 | 16:4,764,078 | A/G | — | uncertain significance |
| rs765380739 | 16:4,764,111 | A/G | — | uncertain significance |
| rs759083239 | 16:4,764,118 | T/A | — | uncertain significance |
| rs141766002 | 16:4,764,163 | G/T | — | uncertain significance |
| rs763204385 | 16:4,764,175 | C/T | — | uncertain significance |
| rs77431482 | 16:4,771,630 | T/G | — | — |
| rs2505658002 | 16:4,774,776 | A/T | — | uncertain significance |
| rs62036061 | 16:4,774,822 | A/C | — | likely benign |
| rs1057519332 | 16:4,776,712 | G/T | — | uncertain significance |
| rs371517379 | 16:4,776,997 | C/T | — | uncertain significance |
| rs149620863 | 16:4,777,018 | T/C | — | uncertain significance |
| rs200665326 | 16:4,777,084 | G/T | — | uncertain significance |
| rs2505674181 | 16:4,777,166 | A/T | — | uncertain significance |
| rs1156341099 | 16:4,779,988 | C/A | — | uncertain significance |
| rs2505690024 | 16:4,780,011 | T/C | — | uncertain significance |
| rs1204689533 | 16:4,780,063 | C/A | — | uncertain significance |
| rs34770007 | 16:4,780,077 | C/T | — | benign |
| rs144184006 | 16:4,780,093 | T/C | — | uncertain significance |
| rs146583899 | 16:4,780,105 | G/A | — | uncertain significance |
| rs140964348 | 16:4,780,109 | C/G | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.