ANKRD30B
ankyrin repeat domain 30B
Known Variants86 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1265221333 | 18:14,748,452 | G/A | — | uncertain significance |
| rs569692334 | 18:14,748,474 | A/G | — | likely benign |
| rs1403895620 | 18:14,748,476 | C/A | — | uncertain significance |
| rs899262751 | 18:14,748,522 | A/G | — | uncertain significance |
| rs375505832 | 18:14,748,578 | C/A | — | uncertain significance |
| rs1329368361 | 18:14,748,632 | A/G | — | uncertain significance |
| rs200428778 | 18:14,752,601 | A/G | — | likely benign |
| rs2510427188 | 18:14,752,865 | G/A | — | uncertain significance |
| rs765818214 | 18:14,752,910 | G/C | — | uncertain significance |
| rs768376526 | 18:14,754,903 | C/A | — | uncertain significance |
| rs536644233 | 18:14,754,944 | A/C | — | uncertain significance |
| rs199720481 | 18:14,754,964 | A/G | — | uncertain significance |
| rs2510437372 | 18:14,754,970 | A/G | — | uncertain significance |
| rs764269719 | 18:14,757,917 | G/C | — | uncertain significance |
| rs371467474 | 18:14,757,923 | C/T | — | uncertain significance |
| rs748290025 | 18:14,763,774 | G/A | — | uncertain significance |
| rs773637187 | 18:14,763,777 | G/A | — | uncertain significance |
| rs755279572 | 18:14,763,870 | C/A | — | uncertain significance |
| rs767015906 | 18:14,763,966 | A/G | — | uncertain significance |
| rs1306988857 | 18:14,764,077 | G/A | — | uncertain significance |
| rs551680231 | 18:14,769,348 | T/A | — | likely benign |
| rs769522759 | 18:14,772,174 | A/G | — | uncertain significance |
| rs1217463346 | 18:14,778,038 | C/A | — | uncertain significance |
| rs769768246 | 18:14,782,539 | G/A | — | uncertain significance |
| rs765269568 | 18:14,784,348 | G/T | — | uncertain significance |
| rs775375669 | 18:14,784,349 | C/T | — | uncertain significance |
| rs921729429 | 18:14,784,350 | C/T | — | uncertain significance |
| rs775465702 | 18:14,784,465 | G/A | — | uncertain significance |
| rs372948852 | 18:14,787,073 | G/A | — | uncertain significance |
| rs376172332 | 18:14,791,446 | C/T | — | uncertain significance |
| rs370663806 | 18:14,791,465 | C/A | — | uncertain significance |
| rs545061007 | 18:14,791,466 | G/A | — | uncertain significance |
| rs768906617 | 18:14,791,475 | A/C | — | uncertain significance |
| rs370210631 | 18:14,796,229 | T/A | — | uncertain significance |
| rs2510622055 | 18:14,796,384 | G/C | — | uncertain significance |
| rs770765402 | 18:14,796,405 | T/C | — | likely benign |
| rs536993823 | 18:14,799,113 | T/A | — | uncertain significance |
| rs747183286 | 18:14,799,232 | G/A | — | uncertain significance |
| rs1969336428 | 18:14,803,757 | A/T | — | uncertain significance |
| rs775216101 | 18:14,803,796 | T/C | — | uncertain significance |
| rs778238896 | 18:14,822,610 | T/C | — | uncertain significance |
| rs987291678 | 18:14,822,611 | G/C | — | uncertain significance |
| rs1970480014 | 18:14,822,628 | C/T | — | uncertain significance |
| rs1209107462 | 18:14,822,649 | T/A | — | uncertain significance |
| rs190308904 | 18:14,826,841 | G/A | upstream gene variant | — |
| rs764204078 | 18:14,828,279 | G/A | — | uncertain significance |
| rs576875141 | 18:14,828,289 | C/T | — | uncertain significance |
| rs188043452 | 18:14,828,291 | G/A | — | uncertain significance |
| rs774373338 | 18:14,831,441 | A/G | — | uncertain significance |
| rs187017186 | 18:14,831,448 | T/C | — | likely benign |
| rs780538017 | 18:14,837,229 | T/C | — | uncertain significance |
| rs1489189867 | 18:14,837,247 | G/A | — | uncertain significance |
| rs2510693896 | 18:14,837,673 | G/A | — | uncertain significance |
| rs1039034131 | 18:14,840,621 | G/A | — | uncertain significance |
| rs571384344 | 18:14,840,674 | G/A | — | uncertain significance |
| rs765665011 | 18:14,843,047 | G/C | — | uncertain significance |
| rs192491310 | 18:14,848,774 | C/T | — | uncertain significance |
| rs199862156 | 18:14,848,849 | G/A | — | uncertain significance |
| rs761007648 | 18:14,848,852 | C/A | — | uncertain significance |
| rs1443319128 | 18:14,848,913 | A/G | — | uncertain significance |
| rs776867847 | 18:14,850,253 | G/A | — | uncertain significance |
| rs2510706539 | 18:14,850,311 | A/G | — | uncertain significance |
| rs745930754 | 18:14,850,329 | C/G | — | uncertain significance |
| rs771727414 | 18:14,850,345 | T/G | — | uncertain significance |
| rs2510706577 | 18:14,850,355 | A/G | — | uncertain significance |
| rs2510707472 | 18:14,851,541 | T/C | — | likely benign |
| rs780048627 | 18:14,851,630 | T/A | — | likely benign |
| rs554299410 | 18:14,851,635 | A/T | — | uncertain significance |
| rs779214321 | 18:14,851,652 | A/T | — | uncertain significance |
| rs774918109 | 18:14,851,701 | A/C | — | uncertain significance |
| rs773934918 | 18:14,851,710 | T/C | — | uncertain significance |
| rs2510707777 | 18:14,851,728 | A/G | — | uncertain significance |
| rs767827578 | 18:14,851,734 | G/A | — | uncertain significance |
| rs563060077 | 18:14,851,749 | T/C | — | uncertain significance |
| rs576681875 | 18:14,851,753 | G/A | — | likely benign |
| rs766906570 | 18:14,851,755 | C/G | — | uncertain significance |
| rs1276832069 | 18:14,852,048 | G/T | — | uncertain significance |
| rs776833055 | 18:14,852,058 | A/T | — | uncertain significance |
| rs1192457400 | 18:14,852,141 | A/G | — | uncertain significance |
| rs770426316 | 18:14,852,169 | A/G | — | uncertain significance |
| rs2510708370 | 18:14,852,220 | A/G | — | uncertain significance |
| rs765182639 | 18:14,852,241 | G/A | — | uncertain significance |
| rs968685351 | 18:14,852,246 | C/A | — | uncertain significance |
| rs2510708483 | 18:14,852,285 | G/C | — | uncertain significance |
| rs200287946 | 18:14,852,325 | G/A | — | likely benign |
| rs1044022884 | 18:14,852,391 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.