ANKRD18A
ankyrin repeat domain 18A
Known Variants64 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs116733635 | 9:38,575,532 | T/C | — | benign |
| rs748551448 | 9:38,575,550 | A/G | — | uncertain significance |
| rs12001355 | 9:38,575,611 | T/C | — | benign |
| rs11999308 | 9:38,575,612 | G/A | — | benign |
| rs760508057 | 9:38,575,622 | T/C | — | uncertain significance |
| rs566758365 | 9:38,577,066 | A/G | — | uncertain significance |
| rs180784545 | 9:38,577,087 | C/T | — | uncertain significance |
| rs2996335 | 9:38,577,101 | G/A | — | uncertain significance |
| rs1417807239 | 9:38,577,133 | C/A | — | likely benign |
| rs535115776 | 9:38,577,167 | C/A | — | uncertain significance |
| rs556870853 | 9:38,577,196 | C/G | — | uncertain significance |
| rs41305300 | 9:38,577,239 | T/G | — | uncertain significance |
| rs2537353696 | 9:38,577,255 | C/T | — | uncertain significance |
| rs748836421 | 9:38,577,914 | C/T | — | uncertain significance |
| rs1424694005 | 9:38,578,004 | T/C | — | uncertain significance |
| rs1823979257 | 9:38,578,012 | T/C | — | uncertain significance |
| rs573746754 | 9:38,578,052 | T/C | — | uncertain significance |
| rs992335891 | 9:38,578,076 | C/T | — | uncertain significance |
| rs1384269574 | 9:38,578,127 | C/T | — | likely benign |
| rs2537357132 | 9:38,578,137 | A/T | — | uncertain significance |
| rs1824372754 | 9:38,586,181 | T/C | — | uncertain significance |
| rs576582593 | 9:38,586,203 | G/C | — | uncertain significance |
| rs547528389 | 9:38,588,572 | C/T | — | likely benign |
| rs1563965896 | 9:38,595,746 | T/C | — | uncertain significance |
| rs2537404572 | 9:38,595,775 | A/C | — | uncertain significance |
| rs1029716726 | 9:38,595,807 | G/T | — | uncertain significance |
| rs540395361 | 9:38,595,820 | C/T | — | uncertain significance |
| rs142963436 | 9:38,596,080 | A/G | — | benign |
| rs147750779 | 9:38,596,117 | T/G | — | benign |
| rs568113286 | 9:38,596,184 | C/A | — | likely benign |
| rs184801559 | 9:38,596,186 | A/T | — | uncertain significance |
| rs1440112686 | 9:38,596,222 | C/T | — | uncertain significance |
| rs746742557 | 9:38,596,255 | C/T | — | uncertain significance |
| rs150333794 | 9:38,596,272 | A/G | — | benign |
| rs200289942 | 9:38,596,294 | C/T | — | likely benign |
| rs1220323213 | 9:38,596,295 | T/C | — | uncertain significance |
| rs958869283 | 9:38,596,300 | T/A | — | uncertain significance |
| rs2537408565 | 9:38,596,370 | C/T | — | uncertain significance |
| rs2537408784 | 9:38,596,400 | C/T | — | uncertain significance |
| rs758505854 | 9:38,601,187 | T/C | — | likely benign |
| rs632223 | 9:38,603,165 | G/A | — | uncertain significance |
| rs1192886249 | 9:38,603,191 | G/A | — | uncertain significance |
| rs773474841 | 9:38,603,192 | G/T | — | uncertain significance |
| rs1388945962 | 9:38,603,209 | T/G | — | uncertain significance |
| rs377760015 | 9:38,607,455 | A/G | — | uncertain significance |
| rs371182398 | 9:38,610,337 | G/A | — | uncertain significance |
| rs141972649 | 9:38,610,359 | G/A | — | benign |
| rs761220501 | 9:38,610,370 | T/C | — | uncertain significance |
| rs759952344 | 9:38,610,381 | T/C | — | uncertain significance |
| rs1388626608 | 9:38,610,388 | C/T | — | uncertain significance |
| rs988551415 | 9:38,611,269 | A/C | — | uncertain significance |
| rs2537448215 | 9:38,611,282 | T/C | — | uncertain significance |
| rs745678894 | 9:38,615,598 | A/G | — | uncertain significance |
| rs1233627185 | 9:38,615,653 | T/C | — | uncertain significance |
| rs750162944 | 9:38,615,694 | T/A | — | uncertain significance |
| rs140456506 | 9:38,616,007 | C/T | — | benign |
| rs373460645 | 9:38,616,016 | G/A | — | likely benign |
| rs191873863 | 9:38,620,069 | C/G | — | benign |
| rs1374691776 | 9:38,620,153 | T/C | — | uncertain significance |
| rs142303885 | 9:38,620,180 | G/A | — | benign |
| rs763398136 | 9:38,620,221 | T/G | — | uncertain significance |
| rs549510583 | 9:38,620,249 | C/A | — | uncertain significance |
| rs1587556065 | 9:38,620,260 | C/G | — | uncertain significance |
| rs1452126854 | 9:38,620,271 | G/A | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.