DLEU7
deleted in lymphocytic leukemia 7
Known Variants29 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1376779234 | 13:51,287,366 | A/G | — | uncertain significance |
| rs523135 | 13:51,321,785 | C/T | intron variant | — |
| rs7988851 | 13:51,367,583 | C/T | intron variant | — |
| rs17478374 | 13:51,369,488 | C/G | intron variant | — |
| rs750176 | 13:51,384,053 | C/T | downstream gene variant | — |
| rs4523838 | 13:51,384,608 | G/A | downstream gene variant | — |
| rs1841677 | 13:51,386,889 | C/T | downstream gene variant | — |
| rs11617827 | 13:51,387,024 | C/A | downstream gene variant | — |
| rs9316505 | 13:51,390,598 | G/A | upstream gene variant | — |
| rs9535499 | 13:51,396,017 | G/A | — | — |
| rs750674028 | 13:51,417,364 | C/T | — | uncertain significance |
| rs375022108 | 13:51,417,397 | G/A | — | uncertain significance |
| rs758939721 | 13:51,417,416 | G/C | — | uncertain significance |
| rs747374364 | 13:51,417,474 | G/T | — | uncertain significance |
| rs766671516 | 13:51,417,545 | C/T | — | uncertain significance |
| rs2541580759 | 13:51,417,555 | A/C | — | uncertain significance |
| rs1455181288 | 13:51,417,569 | C/T | — | uncertain significance |
| rs1286894667 | 13:51,417,587 | C/G | — | uncertain significance |
| rs1281872010 | 13:51,417,596 | G/T | — | uncertain significance |
| rs1443932055 | 13:51,417,601 | G/T | — | uncertain significance |
| rs142725081 | 13:51,417,610 | C/T | — | uncertain significance |
| rs752815935 | 13:51,417,632 | C/T | — | uncertain significance |
| rs759042266 | 13:51,417,638 | C/T | — | uncertain significance |
| rs778394562 | 13:51,417,647 | C/T | — | uncertain significance |
| rs117596350 | 13:51,417,656 | G/T | — | uncertain significance |
| rs775971997 | 13:51,417,670 | C/T | — | uncertain significance |
| rs761070115 | 13:51,417,694 | C/A | — | uncertain significance |
| rs571242579 | 13:51,417,758 | C/A | — | uncertain significance |
| rs1220314912 | 13:51,417,778 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.