SUSD2
sushi domain containing 2
Summary
Involved in negative regulation of cell cycle G1/S phase transition and negative regulation of cell division. Located in plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants90 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs775058351 | 22:24,577,498 | C/A | — | uncertain significance |
| rs115842700 | 22:24,577,531 | C/T | — | benign |
| rs147224860 | 22:24,578,040 | C/T | downstream gene variant | — |
| rs149912020 | 22:24,579,056 | C/T | — | likely benign |
| rs140840148 | 22:24,579,073 | G/A | — | uncertain significance |
| rs768844184 | 22:24,579,084 | C/T | — | uncertain significance |
| rs200621198 | 22:24,579,085 | C/T | — | uncertain significance |
| rs56289213 | 22:24,579,124 | G/C | — | uncertain significance |
| rs566089650 | 22:24,579,171 | G/A | — | uncertain significance |
| rs767392640 | 22:24,579,190 | G/A | — | likely benign |
| rs752884554 | 22:24,579,198 | A/C | — | uncertain significance |
| rs1332235490 | 22:24,579,199 | A/G | — | uncertain significance |
| rs750589882 | 22:24,579,488 | G/A | — | uncertain significance |
| rs138387614 | 22:24,579,548 | C/T | — | uncertain significance |
| rs139630528 | 22:24,579,593 | C/T | — | uncertain significance |
| rs2523652587 | 22:24,579,596 | G/T | — | likely benign |
| rs62642542 | 22:24,579,597 | C/T | — | uncertain significance |
| rs114247596 | 22:24,580,156 | G/A | — | likely benign |
| rs1336199656 | 22:24,580,185 | C/G | — | uncertain significance |
| rs749946904 | 22:24,580,221 | C/G | — | uncertain significance |
| rs1569339736 | 22:24,580,259 | T/A | — | uncertain significance |
| rs190879007 | 22:24,580,616 | C/T | intron variant | — |
| rs201031534 | 22:24,580,770 | C/T | — | uncertain significance |
| rs1285097208 | 22:24,580,775 | C/G | — | uncertain significance |
| rs755005561 | 22:24,580,808 | G/A | — | uncertain significance |
| rs752711134 | 22:24,580,898 | G/A | — | uncertain significance |
| rs373408578 | 22:24,581,066 | G/T | — | uncertain significance |
| rs763053320 | 22:24,581,114 | G/A | — | uncertain significance |
| rs551318370 | 22:24,581,148 | G/A | — | uncertain significance |
| rs145991442 | 22:24,581,193 | A/G | — | likely benign |
| rs145501446 | 22:24,581,211 | C/T | — | uncertain significance |
| rs371492672 | 22:24,581,487 | G/A | — | uncertain significance |
| rs1238378434 | 22:24,581,503 | C/T | — | uncertain significance |
| rs376136602 | 22:24,581,516 | C/T | — | likely benign |
| rs370023790 | 22:24,581,639 | G/A | — | uncertain significance |
| rs147091570 | 22:24,581,650 | G/T | — | uncertain significance |
| rs1569340290 | 22:24,581,664 | C/T | — | uncertain significance |
| rs41304431 | 22:24,581,686 | G/A | — | likely benign |
| rs779090165 | 22:24,581,705 | G/A | — | uncertain significance |
| rs149352625 | 22:24,581,722 | C/T | — | likely benign |
| rs370335967 | 22:24,581,738 | G/A | — | uncertain significance |
| rs377254955 | 22:24,581,745 | C/T | — | uncertain significance |
| rs778008563 | 22:24,581,751 | G/A | — | uncertain significance |
| rs574240131 | 22:24,581,831 | G/A | — | uncertain significance |
| rs770247435 | 22:24,581,846 | A/G | — | uncertain significance |
| rs779714443 | 22:24,581,852 | C/T | — | uncertain significance |
| rs546631132 | 22:24,581,873 | C/T | — | uncertain significance |
| rs1038551745 | 22:24,581,886 | C/T | — | uncertain significance |
| rs2523657954 | 22:24,581,984 | C/A | — | uncertain significance |
| rs2523658000 | 22:24,581,999 | A/C | — | uncertain significance |
| rs8141797 | 22:24,582,041 | A/G | missense variant | benign |
| rs745852076 | 22:24,582,049 | G/A | — | uncertain significance |
| rs143852867 | 22:24,582,082 | G/A | — | uncertain significance |
| rs986781968 | 22:24,582,091 | G/A | — | uncertain significance |
| rs201929646 | 22:24,582,101 | G/A | — | uncertain significance |
| rs369547899 | 22:24,582,123 | C/T | — | likely benign |
| rs115684319 | 22:24,582,236 | C/T | — | benign |
| rs974222200 | 22:24,582,299 | C/A | — | uncertain significance |
| rs140483621 | 22:24,582,314 | G/A | — | likely benign |
| rs1278380931 | 22:24,582,348 | T/C | — | uncertain significance |
| rs779254052 | 22:24,583,184 | G/C | — | uncertain significance |
| rs977064392 | 22:24,583,301 | A/G | — | uncertain significance |
| rs1329207460 | 22:24,583,328 | A/C | — | uncertain significance |
| rs141759016 | 22:24,583,365 | G/A | — | uncertain significance |
| rs762239514 | 22:24,583,374 | C/A | — | uncertain significance |
| rs116712499 | 22:24,583,544 | G/A | — | uncertain significance |
| rs779091820 | 22:24,583,553 | G/T | — | uncertain significance |
| rs748381886 | 22:24,583,554 | C/T | — | uncertain significance |
| rs773767773 | 22:24,583,557 | C/G | — | uncertain significance |
| rs114116915 | 22:24,583,574 | G/A | — | uncertain significance |
| rs752147040 | 22:24,583,586 | C/G | — | uncertain significance |
| rs2047378705 | 22:24,583,627 | C/T | — | likely benign |
| rs372525863 | 22:24,583,631 | G/A | — | uncertain significance |
| rs748222635 | 22:24,583,637 | C/T | — | uncertain significance |
| rs775049884 | 22:24,583,703 | G/A | — | likely benign |
| rs762422172 | 22:24,583,715 | A/G | — | uncertain significance |
| rs763787252 | 22:24,583,716 | A/C | — | uncertain significance |
| rs149333973 | 22:24,583,749 | C/T | — | uncertain significance |
| rs952508715 | 22:24,583,808 | C/G | — | uncertain significance |
| rs149830913 | 22:24,583,953 | C/A | — | uncertain significance |
| rs200013723 | 22:24,583,961 | C/G | — | uncertain significance |
| rs74558263 | 22:24,584,021 | C/T | — | benign |
| rs376889975 | 22:24,584,022 | G/A | — | uncertain significance |
| rs754238872 | 22:24,584,026 | A/G | — | uncertain significance |
| rs1015288858 | 22:24,584,196 | G/A | — | uncertain significance |
| rs750080270 | 22:24,584,204 | G/A | — | likely benign |
| rs142885659 | 22:24,584,235 | T/C | — | uncertain significance |
| rs138048095 | 22:24,584,280 | G/A | — | uncertain significance |
| rs1401312091 | 22:24,584,288 | G/A | — | likely benign |
| rs182282198 | 22:24,585,119 | C/T | downstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.