LAMB4
laminin subunit beta 4
Summary
Predicted to be involved in cell adhesion. Predicted to be located in basement membrane and extracellular region. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants121 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2034752937 | 7:107,664,537 | T/C | — | uncertain significance |
| rs759897739 | 7:107,669,601 | C/T | — | likely benign |
| rs756332022 | 7:107,669,625 | T/C | — | uncertain significance |
| rs2535613571 | 7:107,671,270 | T/C | — | uncertain significance |
| rs779836620 | 7:107,671,289 | C/G | — | uncertain significance |
| rs143043073 | 7:107,671,345 | A/G | — | uncertain significance |
| rs146161342 | 7:107,671,360 | T/C | — | uncertain significance |
| rs2035145623 | 7:107,674,661 | C/T | — | uncertain significance |
| rs569347497 | 7:107,674,671 | T/C | — | uncertain significance |
| rs774333051 | 7:107,674,690 | G/A | — | uncertain significance |
| rs763845029 | 7:107,674,710 | G/T | — | uncertain significance |
| rs748595241 | 7:107,674,735 | G/T | — | uncertain significance |
| rs373331992 | 7:107,677,840 | C/T | — | uncertain significance |
| rs1179948709 | 7:107,677,902 | G/A | — | uncertain significance |
| rs769709242 | 7:107,678,020 | C/G | — | uncertain significance |
| rs1282679671 | 7:107,684,215 | C/T | — | uncertain significance |
| rs142166643 | 7:107,684,224 | T/G | — | uncertain significance |
| rs73424723 | 7:107,684,274 | C/A | — | benign |
| rs765033972 | 7:107,688,369 | C/T | — | uncertain significance |
| rs200655443 | 7:107,688,374 | C/G | — | uncertain significance |
| rs138946711 | 7:107,688,439 | G/A | — | uncertain significance |
| rs2535712860 | 7:107,688,442 | T/G | — | uncertain significance |
| rs765269613 | 7:107,688,460 | C/T | — | likely benign |
| rs187471926 | 7:107,688,495 | G/T | — | uncertain significance |
| rs17134747 | 7:107,688,940 | A/G | intron variant | — |
| rs2535720851 | 7:107,689,790 | A/G | — | uncertain significance |
| rs755446180 | 7:107,689,906 | A/T | — | uncertain significance |
| rs2535721756 | 7:107,689,944 | T/C | — | uncertain significance |
| rs2535721897 | 7:107,689,967 | T/C | — | uncertain significance |
| rs78106755 | 7:107,689,981 | G/A | — | benign |
| rs746859452 | 7:107,692,563 | C/T | — | uncertain significance |
| rs1044897479 | 7:107,692,565 | C/G | — | uncertain significance |
| rs767956550 | 7:107,692,608 | G/A | — | uncertain significance |
| rs1036107808 | 7:107,692,629 | T/C | — | uncertain significance |
| rs149493645 | 7:107,692,681 | A/G | — | benign |
| rs536996128 | 7:107,693,827 | A/T | — | — |
| rs147992634 | 7:107,696,101 | A/C | — | benign |
| rs369035830 | 7:107,696,162 | C/T | — | likely benign |
| rs377464119 | 7:107,696,183 | A/C | — | conflicting classifications of pathogenicity |
| rs373503720 | 7:107,696,248 | C/A | — | uncertain significance |
| rs59354040 | 7:107,696,345 | G/T | — | benign |
| rs79876638 | 7:107,696,352 | G/A | — | benign |
| rs772132232 | 7:107,696,389 | C/A | — | uncertain significance |
| rs367782092 | 7:107,696,394 | C/A | — | uncertain significance |
| rs200242091 | 7:107,696,450 | A/G | — | uncertain significance |
| rs750973233 | 7:107,698,337 | C/T | — | uncertain significance |
| rs144617075 | 7:107,698,357 | G/A | — | uncertain significance |
| rs186813564 | 7:107,700,418 | G/A | intron variant | — |
| rs2535778129 | 7:107,703,227 | A/G | — | uncertain significance |
| rs752103767 | 7:107,703,313 | C/T | — | likely benign |
| rs536424364 | 7:107,703,314 | G/A | — | uncertain significance |
| rs142621710 | 7:107,703,333 | G/A | — | benign |
| rs149661148 | 7:107,703,665 | G/A | regulatory region variant | — |
| rs114388614 | 7:107,704,199 | G/C | — | benign |
| rs754812469 | 7:107,704,214 | G/A | — | uncertain significance |
| rs1015743484 | 7:107,704,274 | G/C | — | uncertain significance |
| rs536192516 | 7:107,704,289 | C/T | — | uncertain significance |
| rs759548666 | 7:107,704,311 | G/A | — | uncertain significance |
| rs752586051 | 7:107,704,322 | T/C | — | uncertain significance |
| rs201060494 | 7:107,704,341 | T/C | — | uncertain significance |
| rs148516927 | 7:107,704,388 | G/A | — | uncertain significance |
| rs760590908 | 7:107,704,419 | C/T | — | uncertain significance |
| rs73725316 | 7:107,706,208 | C/T | — | benign |
| rs144099856 | 7:107,706,259 | A/G | — | likely benign |
| rs146445677 | 7:107,706,317 | C/T | — | uncertain significance |
| rs2535798114 | 7:107,706,829 | C/T | — | uncertain significance |
| rs557671436 | 7:107,706,850 | T/C | — | uncertain significance |
| rs145450595 | 7:107,706,904 | C/A | — | uncertain significance |
| rs148837121 | 7:107,706,946 | C/T | — | uncertain significance |
| rs200608084 | 7:107,707,007 | A/G | — | uncertain significance |
| rs151119551 | 7:107,708,517 | C/T | — | uncertain significance |
| rs201764421 | 7:107,708,533 | G/T | — | uncertain significance |
| rs140790836 | 7:107,708,591 | G/T | — | uncertain significance |
| rs2535816848 | 7:107,710,180 | A/G | — | uncertain significance |
| rs1007334724 | 7:107,710,251 | C/T | — | uncertain significance |
| rs138551579 | 7:107,710,313 | T/C | — | benign |
| rs749961696 | 7:107,717,391 | A/G | — | uncertain significance |
| rs74790077 | 7:107,717,395 | C/T | — | benign |
| rs2535849957 | 7:107,717,441 | G/A | — | uncertain significance |
| rs200365401 | 7:107,717,503 | C/A | — | uncertain significance |
| rs771592925 | 7:107,720,060 | G/A | — | uncertain significance |
| rs145534341 | 7:107,720,070 | G/A | — | benign |
| rs770399713 | 7:107,720,071 | G/A | — | uncertain significance |
| rs138995900 | 7:107,720,172 | A/G | — | benign |
| rs757435046 | 7:107,720,195 | C/T | — | likely benign |
| rs34856038 | 7:107,720,220 | C/T | — | benign |
| rs146912789 | 7:107,720,221 | G/A | — | uncertain significance |
| rs201675880 | 7:107,720,226 | C/T | — | likely benign |
| rs368273128 | 7:107,720,227 | G/A | — | uncertain significance |
| rs147924249 | 7:107,732,072 | A/C | — | uncertain significance |
| rs1225165463 | 7:107,732,142 | A/T | — | uncertain significance |
| rs753356735 | 7:107,732,190 | G/A | — | uncertain significance |
| rs116967479 | 7:107,732,219 | C/A | — | uncertain significance |
| rs34137471 | 7:107,732,826 | C/T | — | benign |
| rs761988518 | 7:107,735,696 | C/T | — | uncertain significance |
| rs1307227339 | 7:107,735,728 | G/A | — | uncertain significance |
| rs1325462553 | 7:107,735,740 | C/T | — | uncertain significance |
| rs142643407 | 7:107,735,764 | A/G | — | uncertain significance |
| rs771256138 | 7:107,738,923 | C/T | — | uncertain significance |
| rs368361747 | 7:107,738,928 | T/C | — | uncertain significance |
Showing 100 of 121 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.