SUSD5
sushi domain containing 5
Summary
Predicted to enable hyaluronic acid binding activity. Predicted to be involved in Notch signaling pathway. Predicted to be located in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants47 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs370876768 | 3:33,194,271 | C/T | — | uncertain significance |
| rs758692164 | 3:33,194,272 | G/C | — | uncertain significance |
| rs1575524898 | 3:33,194,340 | A/G | — | uncertain significance |
| rs768145924 | 3:33,194,397 | A/C | — | uncertain significance |
| rs774564062 | 3:33,194,428 | C/T | — | uncertain significance |
| rs2471607949 | 3:33,194,430 | T/C | — | likely benign |
| rs375235575 | 3:33,194,482 | C/T | — | uncertain significance |
| rs142722850 | 3:33,194,500 | A/G | — | likely benign |
| rs199872747 | 3:33,194,504 | G/T | missense variant | — |
| rs374783367 | 3:33,194,551 | T/C | — | uncertain significance |
| rs916106237 | 3:33,194,579 | C/G | — | uncertain significance |
| rs372702857 | 3:33,194,586 | G/A | — | uncertain significance |
| rs374105402 | 3:33,194,655 | A/G | — | uncertain significance |
| rs1296470798 | 3:33,194,657 | C/A | — | uncertain significance |
| rs755370772 | 3:33,194,745 | A/G | — | uncertain significance |
| rs191836311 | 3:33,194,757 | T/C | — | uncertain significance |
| rs761522971 | 3:33,194,794 | C/A | — | uncertain significance |
| rs200342582 | 3:33,194,838 | T/C | — | uncertain significance |
| rs188571723 | 3:33,194,876 | T/G | — | uncertain significance |
| rs2471608979 | 3:33,194,892 | T/C | — | uncertain significance |
| rs577513217 | 3:33,194,914 | T/G | — | uncertain significance |
| rs200964153 | 3:33,194,938 | C/T | — | uncertain significance |
| rs2030971474 | 3:33,195,093 | T/C | — | uncertain significance |
| rs755874748 | 3:33,195,103 | C/T | — | likely benign |
| rs774020468 | 3:33,195,125 | T/A | — | uncertain significance |
| rs150528777 | 3:33,195,213 | G/A | — | uncertain significance |
| rs75287757 | 3:33,195,264 | C/T | missense variant | — |
| rs767586455 | 3:33,195,379 | G/T | — | uncertain significance |
| rs2030985296 | 3:33,195,401 | A/T | — | likely benign |
| rs189937539 | 3:33,200,114 | C/T | intron variant | — |
| rs4470454 | 3:33,214,146 | C/T | — | — |
| rs2031515799 | 3:33,216,414 | C/G | — | uncertain significance |
| rs763696118 | 3:33,216,462 | T/C | — | likely benign |
| rs2031518525 | 3:33,216,499 | C/A | — | uncertain significance |
| rs1370937539 | 3:33,216,516 | G/A | — | uncertain significance |
| rs189377808 | 3:33,239,379 | C/T | intron variant | — |
| rs201895444 | 3:33,249,308 | T/C | — | uncertain significance |
| rs61744674 | 3:33,249,370 | A/C | — | likely benign |
| rs2471664630 | 3:33,249,371 | G/A | — | uncertain significance |
| rs368720528 | 3:33,255,486 | C/T | — | uncertain significance |
| rs543801064 | 3:33,255,487 | G/A | — | uncertain significance |
| rs376304048 | 3:33,255,517 | C/T | — | uncertain significance |
| rs746556956 | 3:33,255,537 | C/T | — | uncertain significance |
| rs775255479 | 3:33,255,547 | C/T | — | uncertain significance |
| rs185715369 | 3:33,255,558 | C/T | — | uncertain significance |
| rs1282319423 | 3:33,260,196 | G/A | — | uncertain significance |
| rs751258408 | 3:33,260,259 | G/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.