EHBP1L1
EH domain binding protein 1 like 1
Summary
Predicted to act upstream of or within several processes, including enucleation; erythrocyte differentiation; and mitochondrion localization. Located in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants114 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs67924081 | 11:65,342,981 | A/G | regulatory region variant | — |
| rs575137017 | 11:65,343,834 | G/A | — | uncertain significance |
| rs1565116709 | 11:65,343,848 | C/G | — | uncertain significance |
| rs11604423 | 11:65,345,828 | C/G | downstream gene variant | — |
| rs534061165 | 11:65,346,557 | A/G | — | uncertain significance |
| rs547750229 | 11:65,346,583 | C/T | — | uncertain significance |
| rs373275794 | 11:65,346,590 | G/A | — | uncertain significance |
| rs367950334 | 11:65,346,828 | C/T | — | uncertain significance |
| rs749634549 | 11:65,346,848 | C/T | — | uncertain significance |
| rs189053067 | 11:65,346,886 | C/G | — | uncertain significance |
| rs369857321 | 11:65,346,898 | C/G | — | likely benign |
| rs765558377 | 11:65,347,411 | C/T | — | uncertain significance |
| rs776024729 | 11:65,347,573 | G/T | — | uncertain significance |
| rs200464958 | 11:65,347,583 | C/T | — | uncertain significance |
| rs374768138 | 11:65,347,618 | G/A | — | uncertain significance |
| rs746755894 | 11:65,347,621 | C/T | — | uncertain significance |
| rs1353306402 | 11:65,347,673 | T/C | — | uncertain significance |
| rs369730239 | 11:65,347,812 | G/A | — | uncertain significance |
| rs200313831 | 11:65,347,930 | G/A | — | uncertain significance |
| rs370384862 | 11:65,347,936 | G/A | — | likely benign |
| rs201391093 | 11:65,347,942 | C/G | — | uncertain significance |
| rs377050716 | 11:65,347,945 | A/C | — | uncertain significance |
| rs199770292 | 11:65,348,529 | A/G | — | uncertain significance |
| rs199688470 | 11:65,348,736 | C/T | — | uncertain significance |
| rs769519839 | 11:65,348,738 | C/A | — | uncertain significance |
| rs753298411 | 11:65,348,832 | C/T | — | uncertain significance |
| rs756321484 | 11:65,349,056 | C/T | — | uncertain significance |
| rs558905922 | 11:65,349,084 | G/A | — | uncertain significance |
| rs2496304349 | 11:65,349,093 | T/C | — | uncertain significance |
| rs763368746 | 11:65,349,117 | C/T | — | likely benign |
| rs1590819334 | 11:65,349,195 | C/T | — | uncertain significance |
| rs747038078 | 11:65,349,213 | G/A | — | uncertain significance |
| rs561582407 | 11:65,349,216 | T/C | — | likely benign |
| rs745314927 | 11:65,349,227 | A/G | — | uncertain significance |
| rs183233373 | 11:65,349,240 | G/T | — | uncertain significance |
| rs201609538 | 11:65,349,274 | G/A | — | likely benign |
| rs764008468 | 11:65,349,279 | A/T | — | uncertain significance |
| rs2496307698 | 11:65,349,281 | G/A | — | uncertain significance |
| rs1441602858 | 11:65,349,286 | G/A | — | uncertain significance |
| rs1290419458 | 11:65,349,417 | A/G | — | uncertain significance |
| rs1219560847 | 11:65,349,429 | G/C | — | uncertain significance |
| rs368161955 | 11:65,349,452 | A/G | — | uncertain significance |
| rs370393705 | 11:65,349,468 | C/T | — | uncertain significance |
| rs76222487 | 11:65,349,504 | C/T | — | likely benign |
| rs2496311803 | 11:65,349,569 | T/G | — | likely benign |
| rs2496314360 | 11:65,349,710 | C/A | — | uncertain significance |
| rs6591182 | 11:65,349,756 | T/G | missense variant | benign |
| rs1430425199 | 11:65,349,914 | G/A | — | uncertain significance |
| rs370015464 | 11:65,349,926 | C/T | — | uncertain significance |
| rs765424689 | 11:65,349,957 | T/C | — | uncertain significance |
| rs1422962784 | 11:65,350,052 | G/C | — | uncertain significance |
| rs7931269 | 11:65,350,086 | C/T | — | uncertain significance |
| rs202197527 | 11:65,350,146 | C/G | — | uncertain significance |
| rs753655586 | 11:65,350,187 | T/A | — | uncertain significance |
| rs762549962 | 11:65,350,188 | C/G | — | uncertain significance |
| rs758253319 | 11:65,350,194 | A/C | — | uncertain significance |
| rs773266000 | 11:65,350,403 | A/G | — | uncertain significance |
| rs1157841107 | 11:65,350,409 | G/A | — | uncertain significance |
| rs367902486 | 11:65,350,473 | A/T | — | uncertain significance |
| rs1017480643 | 11:65,350,616 | G/C | — | uncertain significance |
| rs1227016230 | 11:65,350,734 | T/G | — | uncertain significance |
| rs370190023 | 11:65,350,742 | C/T | — | uncertain significance |
| rs767111475 | 11:65,350,883 | T/C | — | uncertain significance |
| rs776671963 | 11:65,350,904 | A/G | — | uncertain significance |
| rs1280998654 | 11:65,350,943 | G/A | — | uncertain significance |
| rs761268544 | 11:65,351,034 | C/T | — | uncertain significance |
| rs374766263 | 11:65,351,073 | C/T | — | uncertain significance |
| rs1268478102 | 11:65,351,208 | A/C | — | uncertain significance |
| rs1565126416 | 11:65,351,210 | G/A | — | uncertain significance |
| rs746174380 | 11:65,351,781 | C/T | — | uncertain significance |
| rs564127023 | 11:65,351,787 | G/A | — | uncertain significance |
| rs768779069 | 11:65,351,790 | C/T | — | uncertain significance |
| rs199564079 | 11:65,351,829 | G/C | — | uncertain significance |
| rs185664667 | 11:65,351,863 | A/G | — | uncertain significance |
| rs754188503 | 11:65,351,998 | A/C | — | uncertain significance |
| rs753260817 | 11:65,352,435 | C/G | — | uncertain significance |
| rs201744720 | 11:65,352,458 | T/C | — | uncertain significance |
| rs1414193303 | 11:65,352,493 | C/A | — | uncertain significance |
| rs945676819 | 11:65,352,505 | G/C | — | uncertain significance |
| rs1416059116 | 11:65,352,524 | C/T | — | uncertain significance |
| rs1857882078 | 11:65,352,611 | G/A | — | uncertain significance |
| rs1435178592 | 11:65,352,691 | G/A | — | uncertain significance |
| rs1394583269 | 11:65,352,694 | G/A | — | uncertain significance |
| rs913581552 | 11:65,352,740 | C/T | — | uncertain significance |
| rs1465501258 | 11:65,352,751 | G/T | — | uncertain significance |
| rs757427630 | 11:65,352,890 | G/A | — | uncertain significance |
| rs1462637687 | 11:65,352,917 | G/T | — | uncertain significance |
| rs1857914889 | 11:65,352,929 | C/T | — | uncertain significance |
| rs377298968 | 11:65,352,971 | A/C | — | uncertain significance |
| rs775103367 | 11:65,352,973 | C/G | — | uncertain significance |
| rs1282168194 | 11:65,352,994 | C/G | — | uncertain significance |
| rs370833326 | 11:65,353,021 | A/G | — | likely benign |
| rs569436317 | 11:65,353,040 | G/C | — | uncertain significance |
| rs4601790 | 11:65,353,906 | A/G | downstream gene variant | — |
| rs11606601 | 11:65,354,439 | C/A | — | — |
| rs201994053 | 11:65,357,232 | C/T | — | uncertain significance |
| rs1485548431 | 11:65,357,406 | G/A | — | uncertain significance |
| rs766578309 | 11:65,357,422 | C/T | — | uncertain significance |
| rs765355565 | 11:65,357,561 | C/T | — | uncertain significance |
| rs189205286 | 11:65,357,568 | A/G | — | uncertain significance |
Showing 100 of 114 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.