KLHDC4
kelch domain containing 4
Known Variants68 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs138909472 | 16:87,741,998 | C/T | — | uncertain significance |
| rs199885367 | 16:87,742,004 | C/G | — | uncertain significance |
| rs141766472 | 16:87,742,010 | C/T | — | uncertain significance |
| rs563804177 | 16:87,742,053 | C/A | — | uncertain significance |
| rs984968998 | 16:87,742,891 | G/A | — | likely benign |
| rs781454057 | 16:87,742,900 | G/T | — | likely benign |
| rs370544810 | 16:87,742,951 | C/T | — | uncertain significance |
| rs373948810 | 16:87,742,952 | G/A | — | uncertain significance |
| rs1482795008 | 16:87,742,954 | T/C | — | uncertain significance |
| rs1376659750 | 16:87,742,981 | A/T | — | uncertain significance |
| rs767846001 | 16:87,743,024 | G/A | — | uncertain significance |
| rs367588759 | 16:87,743,027 | G/C | — | uncertain significance |
| rs1394125458 | 16:87,743,048 | T/C | — | likely benign |
| rs377039756 | 16:87,743,051 | C/T | — | likely benign |
| rs2035332332 | 16:87,743,054 | C/A | — | uncertain significance |
| rs1041443500 | 16:87,743,083 | C/T | — | likely benign |
| rs141700495 | 16:87,743,135 | C/T | — | uncertain significance |
| rs2035361181 | 16:87,743,192 | C/G | — | likely benign |
| rs142464429 | 16:87,743,194 | C/A | — | uncertain significance |
| rs772927197 | 16:87,743,199 | A/C | — | uncertain significance |
| rs148870193 | 16:87,743,206 | G/A | — | likely benign |
| rs1014901833 | 16:87,743,243 | G/A | — | uncertain significance |
| rs770378718 | 16:87,743,249 | G/A | — | uncertain significance |
| rs1482771817 | 16:87,743,272 | C/T | — | uncertain significance |
| rs141733244 | 16:87,744,864 | G/A | — | uncertain significance |
| rs374406978 | 16:87,744,876 | C/T | — | uncertain significance |
| rs200058312 | 16:87,744,879 | C/T | — | uncertain significance |
| rs201206196 | 16:87,744,906 | C/T | — | uncertain significance |
| rs113844965 | 16:87,744,911 | G/A | — | uncertain significance |
| rs780438827 | 16:87,744,948 | C/T | — | uncertain significance |
| rs530763969 | 16:87,744,971 | G/A | — | uncertain significance |
| rs534890453 | 16:87,744,974 | G/A | — | uncertain significance |
| rs369702729 | 16:87,744,984 | C/T | — | uncertain significance |
| rs189243168 | 16:87,745,019 | G/A | — | uncertain significance |
| rs753972095 | 16:87,745,031 | C/T | — | uncertain significance |
| rs778845299 | 16:87,745,032 | G/A | — | uncertain significance |
| rs932954224 | 16:87,748,113 | C/T | — | uncertain significance |
| rs764147211 | 16:87,748,140 | C/G | — | uncertain significance |
| rs375679980 | 16:87,748,149 | G/A | — | uncertain significance |
| rs2039437567 | 16:87,760,394 | C/G | — | uncertain significance |
| rs375421008 | 16:87,760,414 | G/A | — | uncertain significance |
| rs751819016 | 16:87,760,447 | G/A | — | uncertain significance |
| rs1168160249 | 16:87,760,519 | T/C | — | uncertain significance |
| rs2040175698 | 16:87,764,206 | G/A | — | uncertain significance |
| rs145431417 | 16:87,764,215 | C/T | — | uncertain significance |
| rs367777769 | 16:87,764,228 | G/A | — | uncertain significance |
| rs756000117 | 16:87,764,248 | G/A | — | uncertain significance |
| rs779800436 | 16:87,764,250 | T/C | — | likely benign |
| rs148640211 | 16:87,782,286 | G/C | — | uncertain significance |
| rs778984427 | 16:87,782,327 | T/C | — | uncertain significance |
| rs139836259 | 16:87,782,397 | C/G | — | uncertain significance |
| rs924255720 | 16:87,788,811 | A/G | — | uncertain significance |
| rs146556886 | 16:87,788,837 | T/C | — | uncertain significance |
| rs2507915226 | 16:87,788,861 | C/A | — | uncertain significance |
| rs141713574 | 16:87,788,876 | T/C | — | uncertain significance |
| rs369024206 | 16:87,788,888 | T/A | — | uncertain significance |
| rs2044912615 | 16:87,790,015 | T/C | — | uncertain significance |
| rs2508028000 | 16:87,795,572 | G/C | — | uncertain significance |
| rs375989397 | 16:87,795,589 | T/G | — | uncertain significance |
| rs2143476917 | 16:87,795,596 | C/A | — | uncertain significance |
| rs139515922 | 16:87,795,600 | T/C | — | likely benign |
| rs955288588 | 16:87,795,613 | T/C | — | uncertain significance |
| rs8061677 | 16:87,797,566 | C/G | — | — |
| rs769219137 | 16:87,799,411 | G/A | — | uncertain significance |
| rs148808761 | 16:87,799,412 | A/G | — | uncertain significance |
| rs780214580 | 16:87,799,463 | G/T | — | uncertain significance |
| rs765224804 | 16:87,799,466 | C/G | — | uncertain significance |
| rs752395417 | 16:87,799,478 | T/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.