SYDE2
synapse defective Rho GTPase homolog 2
Summary
Predicted to enable GTPase activator activity. Acts upstream of or within cell migration. Predicted to be located in cytosol. Predicted to be active in synaptic membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants61 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs765447266 | 1:85,624,846 | G/A | — | uncertain significance |
| rs747587551 | 1:85,630,215 | A/C | — | uncertain significance |
| rs569750698 | 1:85,630,307 | T/G | — | uncertain significance |
| rs191147544 | 1:85,630,428 | T/C | — | uncertain significance |
| rs774443236 | 1:85,634,810 | T/A | — | uncertain significance |
| rs749740486 | 1:85,634,903 | G/T | — | uncertain significance |
| rs61136219 | 1:85,638,617 | G/A | regulatory region variant | — |
| rs779244319 | 1:85,643,825 | T/C | — | uncertain significance |
| rs2526907092 | 1:85,643,852 | T/A | — | uncertain significance |
| rs1490904541 | 1:85,643,903 | C/T | — | uncertain significance |
| rs2526921469 | 1:85,647,814 | T/G | — | uncertain significance |
| rs368885325 | 1:85,647,866 | T/C | — | uncertain significance |
| rs745491934 | 1:85,647,878 | A/G | — | uncertain significance |
| rs774664889 | 1:85,647,899 | T/C | — | likely benign |
| rs753984700 | 1:85,647,918 | G/A | — | uncertain significance |
| rs545962993 | 1:85,647,941 | A/G | — | uncertain significance |
| rs367837897 | 1:85,648,099 | C/G | — | uncertain significance |
| rs767644220 | 1:85,648,226 | T/C | — | uncertain significance |
| rs140672513 | 1:85,648,230 | A/G | — | uncertain significance |
| rs759312339 | 1:85,648,350 | C/T | — | uncertain significance |
| rs746383363 | 1:85,648,446 | G/A | — | uncertain significance |
| rs1657984747 | 1:85,648,504 | T/G | — | uncertain significance |
| rs545541943 | 1:85,648,570 | C/G | — | uncertain significance |
| rs779168336 | 1:85,648,584 | T/C | — | uncertain significance |
| rs1418743754 | 1:85,648,655 | T/G | — | uncertain significance |
| rs561704514 | 1:85,648,703 | C/A | — | uncertain significance |
| rs532048883 | 1:85,648,856 | C/T | — | uncertain significance |
| rs12090608 | 1:85,648,873 | G/C | — | benign |
| rs1252330900 | 1:85,655,782 | T/C | — | uncertain significance |
| rs372217102 | 1:85,655,820 | T/C | — | uncertain significance |
| rs77628096 | 1:85,655,873 | C/T | — | benign |
| rs1408516243 | 1:85,655,889 | T/C | — | uncertain significance |
| rs200884011 | 1:85,655,902 | C/T | — | likely benign |
| rs377055538 | 1:85,655,941 | T/C | — | uncertain significance |
| rs765357248 | 1:85,655,973 | T/C | — | likely benign |
| rs775660312 | 1:85,656,129 | G/A | — | uncertain significance |
| rs2526954064 | 1:85,656,138 | G/A | — | uncertain significance |
| rs781598221 | 1:85,656,196 | A/G | — | likely benign |
| rs746170571 | 1:85,656,199 | G/C | — | uncertain significance |
| rs372874169 | 1:85,656,223 | A/G | — | uncertain significance |
| rs1302920312 | 1:85,656,253 | C/G | — | uncertain significance |
| rs1325963104 | 1:85,656,303 | T/C | — | uncertain significance |
| rs116136609 | 1:85,656,369 | A/G | — | benign |
| rs1371171047 | 1:85,656,375 | T/C | — | uncertain significance |
| rs200529691 | 1:85,656,408 | G/A | — | uncertain significance |
| rs188708420 | 1:85,656,409 | A/G | — | benign |
| rs192842795 | 1:85,656,421 | C/T | — | likely benign |
| rs763791987 | 1:85,656,426 | T/A | — | uncertain significance |
| rs747724631 | 1:85,666,046 | T/A | — | uncertain significance |
| rs1658784750 | 1:85,666,211 | G/A | — | uncertain significance |
| rs376834773 | 1:85,666,251 | C/A | — | uncertain significance |
| rs1658789802 | 1:85,666,283 | G/A | — | uncertain significance |
| rs763283394 | 1:85,666,321 | G/A | — | uncertain significance |
| rs2526990808 | 1:85,666,370 | T/C | — | uncertain significance |
| rs1332291487 | 1:85,666,443 | C/G | — | uncertain significance |
| rs546712035 | 1:85,666,540 | C/T | — | uncertain significance |
| rs749770743 | 1:85,666,579 | G/A | — | uncertain significance |
| rs2526992753 | 1:85,666,604 | C/T | — | uncertain significance |
| rs748480058 | 1:85,666,627 | G/C | — | uncertain significance |
| rs763983350 | 1:85,666,654 | C/A | — | uncertain significance |
| rs1385569506 | 1:85,667,190 | C/T | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.