SBNO2
strawberry notch homolog 2
Summary
Predicted to enable chromatin DNA binding activity and histone binding activity. Involved in several processes, including cellular response to interleukin-6; macrophage activation involved in immune response; and negative regulation of DNA-templated transcription. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants135 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs753053498 | 19:1,108,229 | G/C | — | uncertain significance |
| rs1439591026 | 19:1,108,247 | G/A | — | uncertain significance |
| rs765952457 | 19:1,108,263 | T/A | — | uncertain significance |
| rs1258810930 | 19:1,108,311 | C/T | — | uncertain significance |
| rs775885170 | 19:1,108,338 | G/A | — | uncertain significance |
| rs905841315 | 19:1,108,346 | G/C | — | uncertain significance |
| rs1229183062 | 19:1,108,379 | T/A | — | uncertain significance |
| rs1363633135 | 19:1,108,418 | G/T | — | uncertain significance |
| rs1379906639 | 19:1,108,442 | G/T | — | uncertain significance |
| rs1311285691 | 19:1,108,458 | C/T | — | uncertain significance |
| rs751075868 | 19:1,108,463 | G/C | — | uncertain significance |
| rs1469311830 | 19:1,108,464 | G/A | — | uncertain significance |
| rs754625339 | 19:1,108,466 | C/A | — | uncertain significance |
| rs2079702115 | 19:1,108,469 | G/A | — | uncertain significance |
| rs879438810 | 19:1,108,491 | G/A | — | uncertain significance |
| rs1057169789 | 19:1,108,496 | G/C | — | uncertain significance |
| rs867106126 | 19:1,108,500 | A/C | — | uncertain significance |
| rs887590149 | 19:1,108,529 | G/A | — | uncertain significance |
| rs544160705 | 19:1,108,568 | C/T | — | uncertain significance |
| rs929980963 | 19:1,108,617 | C/T | — | uncertain significance |
| rs765157269 | 19:1,108,801 | G/C | — | uncertain significance |
| rs2512707922 | 19:1,108,954 | C/T | — | uncertain significance |
| rs759537901 | 19:1,108,955 | G/A | — | uncertain significance |
| rs548693130 | 19:1,108,963 | C/T | — | uncertain significance |
| rs1038736914 | 19:1,109,180 | C/T | — | uncertain significance |
| rs544310103 | 19:1,109,340 | C/T | — | uncertain significance |
| rs779866050 | 19:1,109,364 | G/A | — | uncertain significance |
| rs1425066519 | 19:1,109,407 | G/A | — | uncertain significance |
| rs747395050 | 19:1,109,526 | G/T | — | uncertain significance |
| rs1171399033 | 19:1,109,533 | G/T | — | uncertain significance |
| rs759082905 | 19:1,109,539 | G/A | — | uncertain significance |
| rs752493107 | 19:1,109,546 | C/T | — | uncertain significance |
| rs185032569 | 19:1,109,595 | G/T | — | uncertain significance |
| rs375517190 | 19:1,109,702 | C/T | — | uncertain significance |
| rs768132256 | 19:1,109,754 | C/G | — | uncertain significance |
| rs747819146 | 19:1,109,759 | C/T | — | uncertain significance |
| rs2079732154 | 19:1,109,765 | C/T | — | uncertain significance |
| rs778650358 | 19:1,110,796 | G/C | — | uncertain significance |
| rs371986032 | 19:1,110,798 | C/T | — | uncertain significance |
| rs2512716896 | 19:1,111,032 | A/G | — | uncertain significance |
| rs767490708 | 19:1,111,047 | G/A | — | uncertain significance |
| rs780446082 | 19:1,111,091 | G/T | — | uncertain significance |
| rs780352421 | 19:1,111,523 | C/G | — | uncertain significance |
| rs1467046394 | 19:1,111,525 | C/G | — | uncertain significance |
| rs771883775 | 19:1,111,553 | C/T | — | uncertain significance |
| rs2512718833 | 19:1,111,582 | G/T | — | uncertain significance |
| rs2079768852 | 19:1,112,045 | G/A | — | uncertain significance |
| rs763565962 | 19:1,112,271 | C/T | — | uncertain significance |
| rs2512723256 | 19:1,112,406 | T/G | — | uncertain significance |
| rs2512723621 | 19:1,112,466 | T/C | — | uncertain significance |
| rs7249065 | 19:1,112,943 | G/C | — | benign |
| rs370383476 | 19:1,112,944 | G/C | — | uncertain significance |
| rs749333859 | 19:1,113,602 | G/A | — | uncertain significance |
| rs1298598457 | 19:1,113,621 | G/T | — | uncertain significance |
| rs2512729159 | 19:1,113,667 | G/A | — | uncertain significance |
| rs765765176 | 19:1,113,680 | C/T | — | uncertain significance |
| rs936729787 | 19:1,113,692 | G/A | — | uncertain significance |
| rs3746162 | 19:1,114,119 | C/T | regulatory region variant | — |
| rs775103299 | 19:1,114,241 | C/A | — | uncertain significance |
| rs746467821 | 19:1,114,272 | C/T | — | uncertain significance |
| rs1158247590 | 19:1,114,275 | C/T | — | uncertain significance |
| rs2512731543 | 19:1,114,278 | C/T | — | uncertain significance |
| rs768214559 | 19:1,114,304 | T/G | — | uncertain significance |
| rs200891383 | 19:1,114,336 | C/T | — | likely benign |
| rs2512732160 | 19:1,114,371 | C/T | — | uncertain significance |
| rs755089169 | 19:1,114,382 | G/A | — | uncertain significance |
| rs535057070 | 19:1,114,418 | C/T | — | uncertain significance |
| rs777285330 | 19:1,116,846 | C/T | — | uncertain significance |
| rs112316830 | 19:1,116,854 | G/T | — | likely benign |
| rs372053329 | 19:1,116,887 | G/A | — | likely benign |
| rs748768030 | 19:1,117,332 | G/A | — | uncertain significance |
| rs374072609 | 19:1,117,365 | C/T | — | likely benign |
| rs1362938806 | 19:1,117,369 | C/T | — | uncertain significance |
| rs2512743421 | 19:1,117,439 | G/C | — | likely benign |
| rs1335799935 | 19:1,117,452 | C/A | — | uncertain significance |
| rs776595068 | 19:1,117,470 | T/C | — | uncertain significance |
| rs1342345824 | 19:1,119,024 | G/A | — | uncertain significance |
| rs111747553 | 19:1,119,040 | G/A | — | likely benign |
| rs1178886291 | 19:1,119,105 | C/T | — | uncertain significance |
| rs756978453 | 19:1,119,159 | C/T | — | uncertain significance |
| rs748245827 | 19:1,119,551 | C/T | — | uncertain significance |
| rs376127351 | 19:1,119,595 | G/C | — | uncertain significance |
| rs376093678 | 19:1,119,917 | C/T | — | uncertain significance |
| rs775151184 | 19:1,119,964 | G/A | — | uncertain significance |
| rs1251008593 | 19:1,120,022 | T/C | — | uncertain significance |
| rs375408204 | 19:1,122,179 | G/A | — | uncertain significance |
| rs777055488 | 19:1,122,487 | C/T | — | uncertain significance |
| rs765837944 | 19:1,122,495 | G/A | — | uncertain significance |
| rs201293630 | 19:1,122,510 | C/T | — | uncertain significance |
| rs757109846 | 19:1,122,520 | G/A | — | uncertain significance |
| rs554702050 | 19:1,122,550 | C/T | — | uncertain significance |
| rs774785187 | 19:1,122,676 | C/G | — | uncertain significance |
| rs1445409534 | 19:1,122,679 | G/A | — | uncertain significance |
| rs779917708 | 19:1,122,745 | T/G | — | uncertain significance |
| rs751474173 | 19:1,122,906 | G/A | — | uncertain significance |
| rs200890802 | 19:1,122,937 | C/A | — | uncertain significance |
| rs780595324 | 19:1,122,947 | C/T | — | likely benign |
| rs2512763084 | 19:1,122,963 | G/T | — | uncertain significance |
| rs763166442 | 19:1,123,595 | T/A | — | uncertain significance |
| rs2512765437 | 19:1,123,602 | C/T | — | uncertain significance |
Showing 100 of 135 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.