BIN2
bridging integrator 2
Summary
Enables phospholipid binding activity. Involved in several processes, including phagocytosis, engulfment; plasma membrane tubulation; and podosome assembly. Located in phagocytic cup and podosome. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants35 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1945119299 | 12:51,675,287 | A/G | — | uncertain significance |
| rs78506030 | 12:51,677,133 | G/A | intron variant | — |
| rs7306875 | 12:51,679,254 | T/A | intron variant | — |
| rs4611251 | 12:51,681,846 | C/T | intron variant | — |
| rs139691872 | 12:51,681,939 | C/T | — | uncertain significance |
| rs145279960 | 12:51,684,790 | G/A | intron variant | — |
| rs769469897 | 12:51,685,428 | G/A | — | uncertain significance |
| rs758622403 | 12:51,685,535 | A/G | — | uncertain significance |
| rs772997997 | 12:51,685,646 | C/T | — | likely benign |
| rs779658740 | 12:51,685,706 | C/T | — | uncertain significance |
| rs146877980 | 12:51,685,715 | C/T | — | uncertain significance |
| rs1312405207 | 12:51,685,740 | C/T | — | uncertain significance |
| rs375136926 | 12:51,685,776 | C/T | — | likely benign |
| rs1394254714 | 12:51,685,785 | A/T | — | uncertain significance |
| rs369691754 | 12:51,685,842 | G/C | — | uncertain significance |
| rs762467824 | 12:51,685,989 | G/T | — | uncertain significance |
| rs373203887 | 12:51,686,052 | T/C | — | uncertain significance |
| rs1436442266 | 12:51,686,055 | T/G | — | uncertain significance |
| rs370582865 | 12:51,686,063 | G/A | — | uncertain significance |
| rs117491712 | 12:51,686,990 | A/T | intron variant | — |
| rs2359450 | 12:51,687,078 | C/T | — | — |
| rs780678634 | 12:51,689,601 | A/G | — | uncertain significance |
| rs148656859 | 12:51,689,611 | T/A | — | uncertain significance |
| rs7955476 | 12:51,691,551 | A/G | intron variant | — |
| rs7973807 | 12:51,691,952 | T/C | intron variant | — |
| rs200936405 | 12:51,692,997 | G/A | — | uncertain significance |
| rs142121602 | 12:51,693,021 | C/T | missense variant | — |
| rs774127762 | 12:51,693,035 | T/C | — | uncertain significance |
| rs542179917 | 12:51,695,872 | C/T | — | uncertain significance |
| rs751140007 | 12:51,696,498 | C/T | — | uncertain significance |
| rs750169427 | 12:51,696,509 | G/C | — | uncertain significance |
| rs564147412 | 12:51,696,562 | T/C | — | uncertain significance |
| rs766903 | 12:51,703,834 | A/G | intron variant | — |
| rs1051647162 | 12:51,707,672 | C/G | — | uncertain significance |
| rs117053853 | 12:51,720,047 | G/A | upstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.