ARHGAP30
Rho GTPase activating protein 30
Summary
Enables GTPase activator activity. Involved in negative regulation of Rho protein signal transduction. Located in intracellular membrane-bounded organelle. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants58 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs145113918 | 1:161,017,561 | G/A | — | uncertain significance |
| rs929712410 | 1:161,017,594 | G/T | — | uncertain significance |
| rs779729440 | 1:161,017,624 | G/A | — | uncertain significance |
| rs1385915967 | 1:161,017,636 | C/T | — | uncertain significance |
| rs759679526 | 1:161,017,677 | C/T | — | uncertain significance |
| rs1650985016 | 1:161,017,689 | G/A | — | uncertain significance |
| rs1185575374 | 1:161,017,770 | C/T | — | uncertain significance |
| rs1204984373 | 1:161,017,877 | C/G | — | uncertain significance |
| rs747453785 | 1:161,017,903 | G/A | — | uncertain significance |
| rs773189490 | 1:161,017,968 | T/C | — | uncertain significance |
| rs367826999 | 1:161,018,007 | C/T | — | uncertain significance |
| rs748205506 | 1:161,018,043 | C/T | — | uncertain significance |
| rs1433654355 | 1:161,018,074 | A/T | — | uncertain significance |
| rs763630522 | 1:161,018,086 | A/G | — | uncertain significance |
| rs766899947 | 1:161,018,100 | G/C | — | uncertain significance |
| rs771844552 | 1:161,018,158 | T/A | — | uncertain significance |
| rs532517541 | 1:161,018,190 | C/T | — | uncertain significance |
| rs200004996 | 1:161,018,196 | A/C | — | uncertain significance |
| rs758623023 | 1:161,018,299 | G/A | — | uncertain significance |
| rs369546518 | 1:161,018,319 | G/A | — | uncertain significance |
| rs751342626 | 1:161,018,374 | C/T | — | uncertain significance |
| rs143404517 | 1:161,018,392 | A/G | — | uncertain significance |
| rs926811102 | 1:161,018,562 | A/G | — | likely benign |
| rs778382590 | 1:161,018,604 | T/G | — | uncertain significance |
| rs1557915363 | 1:161,018,635 | C/T | — | uncertain significance |
| rs760795163 | 1:161,018,801 | G/C | — | uncertain significance |
| rs2524607004 | 1:161,018,951 | C/T | — | likely benign |
| rs146914272 | 1:161,018,955 | A/G | — | uncertain significance |
| rs772503565 | 1:161,018,992 | C/T | — | uncertain significance |
| rs761202064 | 1:161,019,031 | C/T | — | uncertain significance |
| rs3813609 | 1:161,019,040 | G/T | missense variant | — |
| rs139973145 | 1:161,019,057 | G/A | missense variant | — |
| rs761510561 | 1:161,019,224 | A/C | — | uncertain significance |
| rs774746220 | 1:161,019,236 | T/G | — | uncertain significance |
| rs147106698 | 1:161,019,423 | C/T | — | uncertain significance |
| rs371644392 | 1:161,019,447 | G/T | — | uncertain significance |
| rs562996212 | 1:161,019,472 | C/A | — | uncertain significance |
| rs201733366 | 1:161,021,121 | A/G | — | uncertain significance |
| rs903282972 | 1:161,021,161 | G/A | — | uncertain significance |
| rs748726115 | 1:161,021,190 | C/T | — | uncertain significance |
| rs756442970 | 1:161,021,305 | A/G | — | uncertain significance |
| rs758468847 | 1:161,021,448 | C/T | — | uncertain significance |
| rs781340778 | 1:161,021,465 | G/C | — | uncertain significance |
| rs747945735 | 1:161,021,472 | C/T | — | uncertain significance |
| rs144647339 | 1:161,021,479 | T/C | — | uncertain significance |
| rs1174857511 | 1:161,022,284 | C/G | — | uncertain significance |
| rs754838935 | 1:161,022,484 | T/C | — | uncertain significance |
| rs1474555081 | 1:161,022,543 | C/T | — | uncertain significance |
| rs780252856 | 1:161,022,545 | C/T | — | uncertain significance |
| rs200926712 | 1:161,022,560 | G/A | — | uncertain significance |
| rs146693161 | 1:161,022,569 | C/G | — | uncertain significance |
| rs147495462 | 1:161,023,090 | G/A | — | uncertain significance |
| rs954913816 | 1:161,026,287 | C/T | — | uncertain significance |
| rs143165869 | 1:161,026,302 | C/T | — | uncertain significance |
| rs138526555 | 1:161,029,814 | G/A | intron variant | — |
| rs190590932 | 1:161,032,086 | G/T | upstream gene variant | — |
| rs373555942 | 1:161,039,321 | C/T | — | uncertain significance |
| rs371385714 | 1:161,039,378 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.