SBNO1
strawberry notch homolog 1
Summary
Predicted to enable chromatin DNA binding activity and histone binding activity. Predicted to be involved in several processes, including negative regulation of neuroinflammatory response; positive regulation of neural precursor cell proliferation; and regulation of signal transduction. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants67 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs10846505 | 12:123,775,385 | T/C | upstream gene variant | — |
| rs11057248 | 12:123,781,206 | G/C | intron variant | — |
| rs115621242 | 12:123,782,630 | G/A | — | benign |
| rs113707571 | 12:123,785,526 | A/C | — | — |
| rs10846507 | 12:123,786,492 | G/C | — | — |
| rs61760955 | 12:123,793,863 | T/C | — | benign |
| rs775834999 | 12:123,794,049 | A/G | — | uncertain significance |
| rs147709194 | 12:123,794,093 | A/C | — | uncertain significance |
| rs142553809 | 12:123,794,097 | C/T | — | uncertain significance |
| rs748384962 | 12:123,795,609 | G/A | — | likely benign |
| rs1263014900 | 12:123,795,659 | T/C | — | uncertain significance |
| rs4759375 | 12:123,796,238 | C/T | intron variant | — |
| rs61953423 | 12:123,796,279 | A/C | — | — |
| rs11057258 | 12:123,796,283 | A/G | — | — |
| rs10082867 | 12:123,796,997 | A/G | intron variant | — |
| rs2547644809 | 12:123,798,185 | G/T | — | uncertain significance |
| rs12317103 | 12:123,802,814 | T/C | intron variant | — |
| rs924780430 | 12:123,804,508 | A/G | — | uncertain significance |
| rs774812067 | 12:123,804,544 | T/C | — | uncertain significance |
| rs2547652012 | 12:123,804,547 | T/C | — | uncertain significance |
| rs12366872 | 12:123,804,721 | G/C | intron variant | — |
| rs149772827 | 12:123,805,035 | G/C | — | uncertain significance |
| rs371938704 | 12:123,805,133 | T/C | — | uncertain significance |
| rs61760909 | 12:123,805,261 | G/A | — | benign |
| rs2547653023 | 12:123,805,285 | A/T | — | uncertain significance |
| rs114314586 | 12:123,806,084 | T/C | — | likely benign |
| rs374595184 | 12:123,806,183 | T/C | — | uncertain significance |
| rs1869990261 | 12:123,806,223 | T/A | — | uncertain significance |
| rs372233667 | 12:123,806,241 | C/T | — | uncertain significance |
| rs146861005 | 12:123,806,283 | C/T | — | benign |
| rs1234885150 | 12:123,808,280 | T/C | — | uncertain significance |
| rs752027264 | 12:123,810,738 | C/G | — | uncertain significance |
| rs1566037478 | 12:123,810,863 | G/A | — | uncertain significance |
| rs369659618 | 12:123,810,878 | C/T | — | uncertain significance |
| rs75710010 | 12:123,812,129 | G/A | — | benign |
| rs2547660992 | 12:123,812,273 | T/C | — | uncertain significance |
| rs200446829 | 12:123,812,295 | T/C | — | benign |
| rs1593370095 | 12:123,812,560 | C/T | — | likely benign |
| rs2547662470 | 12:123,813,348 | G/C | — | uncertain significance |
| rs11057273 | 12:123,814,466 | T/A | — | — |
| rs2547664096 | 12:123,814,968 | T/C | — | uncertain significance |
| rs2547664114 | 12:123,814,985 | A/G | — | uncertain significance |
| rs140771058 | 12:123,814,987 | A/C | — | uncertain significance |
| rs1280372720 | 12:123,815,843 | G/A | — | uncertain significance |
| rs11611694 | 12:123,817,649 | C/T | intron variant | — |
| rs145199462 | 12:123,818,738 | T/C | — | likely benign |
| rs140801858 | 12:123,820,980 | C/A | — | uncertain significance |
| rs1199218621 | 12:123,821,034 | A/G | — | uncertain significance |
| rs7980687 | 12:123,822,711 | G/T | — | — |
| rs11830103 | 12:123,823,546 | A/G | intron variant | — |
| rs67624109 | 12:123,824,635 | C/T | intron variant | — |
| rs201237443 | 12:123,825,602 | G/T | — | uncertain significance |
| rs116725625 | 12:123,825,635 | G/A | — | benign |
| rs118119987 | 12:123,825,640 | G/A | — | benign |
| rs369036168 | 12:123,829,837 | G/C | — | uncertain significance |
| rs1433527761 | 12:123,829,888 | T/A | — | uncertain significance |
| rs749917194 | 12:123,829,963 | C/T | — | uncertain significance |
| rs778836779 | 12:123,829,970 | T/C | — | uncertain significance |
| rs886262380 | 12:123,830,014 | T/C | — | uncertain significance |
| rs377064185 | 12:123,830,063 | G/A | — | uncertain significance |
| rs7298909 | 12:123,830,939 | C/T | downstream gene variant | — |
| rs9300255 | 12:123,833,521 | T/A | — | — |
| rs193920847 | 12:123,834,853 | T/G | — | uncertain significance |
| rs748779441 | 12:123,834,874 | T/C | — | uncertain significance |
| rs9668827 | 12:123,843,017 | C/T | intron variant | — |
| rs28376696 | 12:123,849,863 | T/C | coding sequence variant | — |
| rs61955089 | 12:123,851,372 | T/C | upstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.