SGSM3
small G protein signaling modulator 3
Summary
Enables GTPase activator activity and small GTPase binding activity. Involved in several processes, including Rap protein signal transduction; positive regulation of GTPase activity; and regulation of Rab protein signal transduction. Located in cytosol. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants78 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs895069567 | 22:40,797,600 | G/A | — | uncertain significance |
| rs2518355965 | 22:40,797,621 | C/T | — | uncertain significance |
| rs9611338 | 22:40,797,647 | T/C | — | benign |
| rs991602621 | 22:40,800,271 | A/C | — | uncertain significance |
| rs758930073 | 22:40,800,281 | C/T | — | uncertain significance |
| rs777546956 | 22:40,800,304 | G/A | — | uncertain significance |
| rs73420601 | 22:40,800,320 | G/A | — | uncertain significance |
| rs2518381332 | 22:40,800,364 | G/A | — | uncertain significance |
| rs143730708 | 22:40,800,400 | C/T | — | likely benign |
| rs141250350 | 22:40,800,571 | G/A | — | uncertain significance |
| rs1002565374 | 22:40,800,616 | A/G | — | uncertain significance |
| rs374291042 | 22:40,800,618 | C/T | — | uncertain significance |
| rs564483084 | 22:40,800,621 | G/C | — | uncertain significance |
| rs2518384908 | 22:40,800,636 | A/G | — | uncertain significance |
| rs142415355 | 22:40,800,645 | G/A | — | uncertain significance |
| rs2518390620 | 22:40,801,151 | A/C | — | uncertain significance |
| rs144524421 | 22:40,801,181 | G/A | — | uncertain significance |
| rs756348980 | 22:40,801,190 | G/A | — | uncertain significance |
| rs150525363 | 22:40,801,207 | C/T | — | benign |
| rs746644745 | 22:40,801,208 | G/A | — | uncertain significance |
| rs767686797 | 22:40,801,235 | C/T | — | uncertain significance |
| rs753127820 | 22:40,801,236 | G/A | — | uncertain significance |
| rs369794718 | 22:40,801,264 | C/T | — | likely benign |
| rs12483888 | 22:40,801,312 | A/G | downstream gene variant | — |
| rs202194574 | 22:40,801,688 | G/C | — | uncertain significance |
| rs565900842 | 22:40,801,690 | A/C | — | uncertain significance |
| rs368788322 | 22:40,801,707 | T/C | — | uncertain significance |
| rs141654422 | 22:40,801,787 | G/C | — | benign |
| rs763742049 | 22:40,801,788 | C/T | — | uncertain significance |
| rs1015170395 | 22:40,801,798 | T/C | — | uncertain significance |
| rs555539426 | 22:40,801,816 | G/A | — | uncertain significance |
| rs746363143 | 22:40,802,086 | G/A | — | likely benign |
| rs2518403449 | 22:40,802,095 | C/G | — | uncertain significance |
| rs202034135 | 22:40,802,115 | C/T | — | uncertain significance |
| rs376746554 | 22:40,802,129 | G/A | — | uncertain significance |
| rs1261824170 | 22:40,802,132 | G/A | — | likely benign |
| rs142323976 | 22:40,802,134 | G/A | — | likely benign |
| rs369644750 | 22:40,802,179 | G/C | — | uncertain significance |
| rs375708190 | 22:40,802,497 | A/T | — | uncertain significance |
| rs200407927 | 22:40,802,520 | G/A | — | uncertain significance |
| rs141140445 | 22:40,802,548 | G/A | — | uncertain significance |
| rs199844144 | 22:40,802,567 | C/T | — | likely benign |
| rs150705401 | 22:40,802,576 | C/T | — | likely benign |
| rs368831798 | 22:40,802,577 | G/A | — | uncertain significance |
| rs772300191 | 22:40,802,590 | G/A | — | uncertain significance |
| rs139978626 | 22:40,802,631 | C/T | — | uncertain significance |
| rs1249659525 | 22:40,802,640 | G/A | — | likely benign |
| rs752442418 | 22:40,802,643 | G/A | — | likely benign |
| rs558698128 | 22:40,803,031 | G/A | — | uncertain significance |
| rs150363308 | 22:40,803,041 | G/A | — | likely benign |
| rs2018393 | 22:40,803,186 | T/G | — | benign |
| rs202226045 | 22:40,803,288 | G/A | — | uncertain significance |
| rs369422074 | 22:40,803,295 | G/A | — | uncertain significance |
| rs140395314 | 22:40,803,303 | C/A | — | uncertain significance |
| rs778768668 | 22:40,803,448 | A/T | — | uncertain significance |
| rs2518423223 | 22:40,803,463 | A/G | — | uncertain significance |
| rs140993538 | 22:40,803,471 | G/A | — | uncertain significance |
| rs200569646 | 22:40,803,478 | G/A | — | uncertain significance |
| rs563225500 | 22:40,803,483 | C/T | — | uncertain significance |
| rs1455506419 | 22:40,803,495 | C/T | — | uncertain significance |
| rs376663138 | 22:40,803,553 | G/A | — | uncertain significance |
| rs2518433209 | 22:40,804,107 | G/A | — | uncertain significance |
| rs760678093 | 22:40,804,309 | C/T | — | uncertain significance |
| rs780033716 | 22:40,804,359 | G/T | — | uncertain significance |
| rs371726297 | 22:40,804,404 | G/A | — | uncertain significance |
| rs61729163 | 22:40,804,412 | C/T | — | benign |
| rs773465107 | 22:40,804,640 | C/T | — | uncertain significance |
| rs117951659 | 22:40,804,641 | G/A | — | uncertain significance |
| rs765956501 | 22:40,804,667 | G/A | — | uncertain significance |
| rs755966818 | 22:40,804,676 | C/T | — | uncertain significance |
| rs775361941 | 22:40,804,811 | G/A | — | uncertain significance |
| rs137920402 | 22:40,804,845 | G/A | — | uncertain significance |
| rs115360539 | 22:40,804,932 | C/A | — | benign |
| rs773271072 | 22:40,804,997 | C/T | — | uncertain significance |
| rs745981773 | 22:40,805,304 | C/T | — | uncertain significance |
| rs138537467 | 22:40,805,305 | C/T | — | likely benign |
| rs1017134561 | 22:40,805,492 | G/A | — | uncertain significance |
| rs200774462 | 22:40,805,714 | G/A | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.