SUSD1
sushi domain containing 1
Summary
Predicted to enable calcium ion binding activity. Predicted to be located in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants66 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs773432036 | 9:114,804,151 | C/T | — | uncertain significance |
| rs374874509 | 9:114,804,166 | G/A | — | uncertain significance |
| rs146843448 | 9:114,804,191 | C/T | — | likely benign |
| rs780435594 | 9:114,804,211 | C/T | — | uncertain significance |
| rs990595595 | 9:114,814,687 | T/G | — | uncertain significance |
| rs376263591 | 9:114,820,725 | T/C | — | uncertain significance |
| rs757665047 | 9:114,820,777 | A/G | — | likely benign |
| rs765774346 | 9:114,820,881 | C/T | — | likely benign |
| rs377416608 | 9:114,820,902 | C/A | — | uncertain significance |
| rs2538201205 | 9:114,820,919 | G/T | — | uncertain significance |
| rs79461840 | 9:114,822,158 | T/C | regulatory region variant | — |
| rs4979078 | 9:114,823,121 | T/C | intron variant | — |
| rs542533485 | 9:114,823,308 | C/T | — | — |
| rs80215167 | 9:114,825,299 | C/T | — | likely benign |
| rs2762502 | 9:114,835,479 | T/C | regulatory region variant | — |
| rs6477879 | 9:114,840,642 | G/A | intron variant | — |
| rs147151457 | 9:114,840,837 | G/A | — | likely benign |
| rs906390812 | 9:114,840,866 | G/C | — | uncertain significance |
| rs765406042 | 9:114,840,898 | G/A | — | uncertain significance |
| rs764469249 | 9:114,840,902 | G/A | — | uncertain significance |
| rs1361085308 | 9:114,840,938 | T/C | — | uncertain significance |
| rs61120558 | 9:114,842,160 | A/G | intron variant | — |
| rs60956063 | 9:114,842,453 | G/A | — | benign |
| rs2782931 | 9:114,850,190 | C/G | — | — |
| rs2564898 | 9:114,850,947 | T/A | — | — |
| rs149272609 | 9:114,860,789 | G/A | — | uncertain significance |
| rs759398570 | 9:114,860,804 | G/C | — | uncertain significance |
| rs201816303 | 9:114,860,817 | C/A | — | likely benign |
| rs373423817 | 9:114,860,870 | C/T | — | uncertain significance |
| rs750560741 | 9:114,860,872 | C/T | — | uncertain significance |
| rs144111205 | 9:114,860,894 | T/C | — | uncertain significance |
| rs748822288 | 9:114,860,897 | C/A | — | uncertain significance |
| rs1830499072 | 9:114,860,903 | A/G | — | uncertain significance |
| rs763423439 | 9:114,864,491 | G/A | — | uncertain significance |
| rs146484239 | 9:114,864,492 | C/A | — | uncertain significance |
| rs146611081 | 9:114,873,997 | C/T | — | benign |
| rs754168237 | 9:114,874,081 | C/T | — | uncertain significance |
| rs779392704 | 9:114,874,092 | G/A | — | uncertain significance |
| rs1831673186 | 9:114,886,553 | A/T | — | uncertain significance |
| rs146879704 | 9:114,886,569 | C/T | missense variant | — |
| rs774815840 | 9:114,886,635 | C/T | — | likely benign |
| rs148200019 | 9:114,886,636 | G/A | — | uncertain significance |
| rs372453127 | 9:114,886,645 | C/G | — | uncertain significance |
| rs745698844 | 9:114,886,686 | C/T | — | likely benign |
| rs7849537 | 9:114,897,899 | T/C | upstream gene variant | — |
| rs66478924 | 9:114,900,122 | G/A | coding sequence variant | — |
| rs112182189 | 9:114,900,500 | T/A | — | — |
| rs142035069 | 9:114,902,628 | G/A | — | — |
| rs1277423095 | 9:114,904,699 | G/A | — | uncertain significance |
| rs17829458 | 9:114,904,705 | G/C | — | likely benign |
| rs372823319 | 9:114,904,764 | G/A | — | uncertain significance |
| rs143390223 | 9:114,905,753 | G/A | — | benign |
| rs369141407 | 9:114,905,769 | C/T | — | uncertain significance |
| rs1029867596 | 9:114,905,787 | G/A | — | uncertain significance |
| rs760395542 | 9:114,905,853 | C/T | — | uncertain significance |
| rs142288874 | 9:114,911,551 | T/A | — | uncertain significance |
| rs75423111 | 9:114,911,591 | G/A | — | benign |
| rs769688623 | 9:114,911,611 | C/T | — | uncertain significance |
| rs139750662 | 9:114,911,635 | G/A | — | uncertain significance |
| rs150275769 | 9:114,919,799 | G/A | — | benign |
| rs138958002 | 9:114,919,819 | T/G | — | uncertain significance |
| rs115339119 | 9:114,919,886 | G/A | — | benign |
| rs10817274 | 9:114,929,971 | G/A | upstream gene variant | — |
| rs10981292 | 9:114,930,574 | G/A | regulatory region variant | — |
| rs2538814411 | 9:114,937,484 | G/A | — | uncertain significance |
| rs1390910983 | 9:114,937,493 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.