KLHL33
kelch like family member 33
Known Variants54 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1713450 | 14:20,896,245 | T/C | regulatory region variant | — |
| rs982908797 | 14:20,897,016 | C/A | — | uncertain significance |
| rs201783825 | 14:20,897,112 | G/T | — | uncertain significance |
| rs777027130 | 14:20,897,123 | C/A | — | uncertain significance |
| rs372057023 | 14:20,897,132 | C/T | — | uncertain significance |
| rs188099735 | 14:20,897,183 | C/T | — | conflicting classifications of pathogenicity |
| rs1045252007 | 14:20,897,189 | C/T | — | uncertain significance |
| rs372157970 | 14:20,897,247 | G/T | — | uncertain significance |
| rs966421468 | 14:20,897,297 | T/C | — | uncertain significance |
| rs866215214 | 14:20,897,334 | G/T | — | uncertain significance |
| rs78943907 | 14:20,897,387 | C/T | — | uncertain significance |
| rs753967346 | 14:20,897,417 | C/T | — | uncertain significance |
| rs1354607124 | 14:20,897,420 | G/A | — | uncertain significance |
| rs2502582307 | 14:20,897,517 | C/T | — | uncertain significance |
| rs369968163 | 14:20,897,667 | A/G | — | uncertain significance |
| rs370206398 | 14:20,897,670 | T/G | — | uncertain significance |
| rs565567891 | 14:20,897,715 | T/C | — | uncertain significance |
| rs1312557474 | 14:20,897,727 | C/T | — | uncertain significance |
| rs199726282 | 14:20,897,737 | A/T | — | uncertain significance |
| rs957559793 | 14:20,897,824 | C/T | — | uncertain significance |
| rs1440086764 | 14:20,897,828 | C/T | — | likely benign |
| rs1566499503 | 14:20,897,984 | C/T | — | uncertain significance |
| rs1880434407 | 14:20,898,035 | G/A | — | uncertain significance |
| rs952999124 | 14:20,898,047 | C/T | — | uncertain significance |
| rs773483540 | 14:20,898,059 | G/A | — | uncertain significance |
| rs953779386 | 14:20,898,120 | G/A | — | likely benign |
| rs375936916 | 14:20,898,124 | G/T | — | likely benign |
| rs996119781 | 14:20,898,129 | G/A | — | uncertain significance |
| rs369825651 | 14:20,898,146 | C/G | — | uncertain significance |
| rs1299135816 | 14:20,898,153 | G/A | — | uncertain significance |
| rs1376112672 | 14:20,898,158 | C/G | — | uncertain significance |
| rs961786041 | 14:20,898,201 | C/T | — | uncertain significance |
| rs143863859 | 14:20,898,225 | G/A | — | uncertain significance |
| rs1016575504 | 14:20,898,237 | C/T | — | uncertain significance |
| rs1463497404 | 14:20,898,269 | A/G | — | uncertain significance |
| rs546054192 | 14:20,898,309 | G/A | — | uncertain significance |
| rs758196679 | 14:20,898,317 | C/T | — | uncertain significance |
| rs774326348 | 14:20,898,318 | G/A | — | uncertain significance |
| rs866492022 | 14:20,898,339 | G/A | — | uncertain significance |
| rs543538009 | 14:20,898,348 | G/A | — | uncertain significance |
| rs529289338 | 14:20,898,356 | C/T | — | likely benign |
| rs970989153 | 14:20,898,404 | A/G | — | uncertain significance |
| rs962384556 | 14:20,898,414 | G/A | — | uncertain significance |
| rs550721927 | 14:20,898,435 | A/T | — | uncertain significance |
| rs2502588580 | 14:20,898,476 | G/A | — | uncertain significance |
| rs551271666 | 14:20,898,522 | C/G | — | uncertain significance |
| rs374640394 | 14:20,898,536 | G/A | — | uncertain significance |
| rs1370759340 | 14:20,898,548 | T/C | — | uncertain significance |
| rs45448391 | 14:20,898,585 | C/T | — | uncertain significance |
| rs567375766 | 14:20,898,669 | A/G | — | uncertain significance |
| rs749594652 | 14:20,898,725 | C/T | — | uncertain significance |
| rs1003212014 | 14:20,898,735 | C/T | — | uncertain significance |
| rs376086238 | 14:20,898,761 | C/A | — | uncertain significance |
| rs1399315310 | 14:20,898,782 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.