ANKRD33B
ankyrin repeat domain 33B
Known Variants45 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1386144197 | 5:10,564,632 | C/T | — | uncertain significance |
| rs1299159890 | 5:10,564,653 | C/G | — | uncertain significance |
| rs925028453 | 5:10,564,710 | C/G | — | uncertain significance |
| rs779496788 | 5:10,564,790 | A/G | — | uncertain significance |
| rs2478747695 | 5:10,564,827 | T/G | — | uncertain significance |
| rs1318760337 | 5:10,564,934 | C/A | — | uncertain significance |
| rs1218793103 | 5:10,564,935 | G/C | — | uncertain significance |
| rs574173815 | 5:10,573,505 | C/T | — | — |
| rs773162015 | 5:10,618,448 | G/A | — | uncertain significance |
| rs1231471846 | 5:10,618,487 | G/C | — | uncertain significance |
| rs746481449 | 5:10,618,506 | G/A | — | uncertain significance |
| rs1017880946 | 5:10,618,526 | T/G | — | uncertain significance |
| rs10035875 | 5:10,623,653 | G/A | — | — |
| rs758987186 | 5:10,638,154 | A/G | — | uncertain significance |
| rs1737262277 | 5:10,649,378 | G/T | — | uncertain significance |
| rs772112224 | 5:10,649,471 | A/G | — | uncertain significance |
| rs941979241 | 5:10,649,476 | C/A | — | uncertain significance |
| rs1328708498 | 5:10,649,485 | C/T | — | uncertain significance |
| rs1037300195 | 5:10,649,540 | C/T | — | uncertain significance |
| rs1056953871 | 5:10,649,560 | G/A | — | uncertain significance |
| rs1737273307 | 5:10,649,597 | G/T | — | likely benign |
| rs865834509 | 5:10,649,599 | G/C | — | likely benign |
| rs768074427 | 5:10,649,618 | C/T | — | uncertain significance |
| rs967396208 | 5:10,649,641 | G/A | — | uncertain significance |
| rs1380722237 | 5:10,649,711 | G/C | — | uncertain significance |
| rs1202693998 | 5:10,649,731 | A/G | — | uncertain significance |
| rs1240693470 | 5:10,649,733 | C/A | — | uncertain significance |
| rs1737281780 | 5:10,649,734 | C/T | — | uncertain significance |
| rs549928232 | 5:10,649,738 | C/T | — | uncertain significance |
| rs769639573 | 5:10,649,783 | C/T | — | uncertain significance |
| rs904277765 | 5:10,649,801 | C/T | — | uncertain significance |
| rs1054801792 | 5:10,649,809 | C/A | — | uncertain significance |
| rs1000222233 | 5:10,649,848 | C/T | — | uncertain significance |
| rs1473337656 | 5:10,649,858 | A/G | — | uncertain significance |
| rs996240906 | 5:10,649,864 | A/G | — | uncertain significance |
| rs112597450 | 5:10,649,882 | G/A | — | uncertain significance |
| rs181259002 | 5:10,649,902 | C/T | — | uncertain significance |
| rs1484900169 | 5:10,649,903 | C/T | — | uncertain significance |
| rs931164290 | 5:10,649,938 | G/T | — | likely benign |
| rs902186415 | 5:10,650,020 | G/T | — | uncertain significance |
| rs112072949 | 5:10,650,090 | C/A | — | uncertain significance |
| rs750484899 | 5:10,650,103 | A/C | — | likely benign |
| rs952656310 | 5:10,650,136 | G/A | — | uncertain significance |
| rs916450980 | 5:10,650,161 | A/C | — | uncertain significance |
| rs1403322640 | 5:10,650,197 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.