KLHL26
kelch like family member 26
Known Variants35 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs3764628 | 19:18,747,605 | G/T | regulatory region variant | — |
| rs987301920 | 19:18,747,869 | C/T | — | uncertain significance |
| rs1369890534 | 19:18,747,923 | G/A | — | uncertain significance |
| rs1039574984 | 19:18,747,945 | C/G | — | uncertain significance |
| rs12974777 | 19:18,765,663 | C/T | intron variant | — |
| rs568250280 | 19:18,775,177 | G/C | — | uncertain significance |
| rs368361177 | 19:18,775,225 | G/A | — | uncertain significance |
| rs752461758 | 19:18,775,243 | G/A | — | uncertain significance |
| rs144914430 | 19:18,778,514 | G/A | — | likely benign |
| rs774411539 | 19:18,778,533 | T/A | — | uncertain significance |
| rs373143236 | 19:18,778,559 | A/G | — | uncertain significance |
| rs559660346 | 19:18,778,814 | C/T | — | uncertain significance |
| rs140820566 | 19:18,778,840 | C/T | — | likely benign |
| rs2513453107 | 19:18,778,878 | T/C | — | uncertain significance |
| rs746579789 | 19:18,778,926 | G/A | — | uncertain significance |
| rs1311791204 | 19:18,778,952 | T/C | — | uncertain significance |
| rs1416272701 | 19:18,778,958 | A/G | — | uncertain significance |
| rs775736569 | 19:18,778,980 | C/G | — | uncertain significance |
| rs1019937400 | 19:18,778,997 | A/G | — | uncertain significance |
| rs147255312 | 19:18,779,064 | A/G | — | uncertain significance |
| rs773255884 | 19:18,779,085 | G/A | — | uncertain significance |
| rs754382650 | 19:18,779,124 | C/T | — | uncertain significance |
| rs751924313 | 19:18,779,310 | G/A | — | uncertain significance |
| rs2513454943 | 19:18,779,394 | T/C | — | uncertain significance |
| rs1233713323 | 19:18,779,468 | C/T | — | uncertain significance |
| rs766702905 | 19:18,779,490 | C/T | — | uncertain significance |
| rs1168841838 | 19:18,779,498 | G/A | — | uncertain significance |
| rs950751881 | 19:18,779,519 | A/G | — | uncertain significance |
| rs2513455621 | 19:18,779,587 | C/A | — | likely benign |
| rs1263665885 | 19:18,779,588 | C/T | — | uncertain significance |
| rs199645016 | 19:18,779,631 | A/G | — | uncertain significance |
| rs2513455889 | 19:18,779,672 | G/C | — | uncertain significance |
| rs201261086 | 19:18,779,814 | C/G | — | uncertain significance |
| rs1364965574 | 19:18,780,018 | C/T | — | uncertain significance |
| rs371571391 | 19:18,780,020 | C/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.