ARHGEF38
Rho guanine nucleotide exchange factor 38
Summary
Predicted to enable guanyl-nucleotide exchange factor activity. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants45 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs375204038 | 4:106,473,975 | A/G | — | uncertain significance |
| rs146139851 | 4:106,473,991 | G/T | — | uncertain significance |
| rs77566495 | 4:106,510,429 | G/T | — | uncertain significance |
| rs2476270681 | 4:106,510,443 | A/T | — | uncertain significance |
| rs2476270994 | 4:106,510,498 | A/C | — | uncertain significance |
| rs765574141 | 4:106,510,540 | A/G | — | uncertain significance |
| rs974914156 | 4:106,534,586 | G/A | — | uncertain significance |
| rs61751053 | 4:106,534,599 | C/T | missense variant | — |
| rs771840583 | 4:106,534,635 | C/T | — | uncertain significance |
| rs34152356 | 4:106,552,118 | A/G | — | uncertain significance |
| rs200568523 | 4:106,552,163 | A/G | — | uncertain significance |
| rs772495615 | 4:106,552,189 | A/G | — | uncertain significance |
| rs17036027 | 4:106,556,518 | C/A | — | — |
| rs564248049 | 4:106,556,654 | T/C | — | — |
| rs572288838 | 4:106,566,380 | T/C | — | uncertain significance |
| rs1402408053 | 4:106,566,381 | G/A | — | uncertain significance |
| rs1202582797 | 4:106,566,427 | G/A | — | uncertain significance |
| rs773873939 | 4:106,566,433 | C/T | — | uncertain significance |
| rs1375328586 | 4:106,566,537 | A/C | — | uncertain significance |
| rs138832734 | 4:106,569,810 | C/T | — | likely benign |
| rs569008337 | 4:106,575,232 | A/G | — | uncertain significance |
| rs1018354670 | 4:106,575,316 | A/G | — | uncertain significance |
| rs757874020 | 4:106,576,821 | A/T | — | uncertain significance |
| rs960214528 | 4:106,576,823 | G/A | — | uncertain significance |
| rs2476483846 | 4:106,576,836 | A/G | — | uncertain significance |
| rs773225753 | 4:106,576,856 | G/A | — | uncertain significance |
| rs1982346 | 4:106,578,754 | A/G | regulatory region variant | — |
| rs557583930 | 4:106,580,230 | T/A | — | uncertain significance |
| rs1417009054 | 4:106,580,257 | T/C | — | uncertain significance |
| rs1051796195 | 4:106,580,335 | G/A | — | uncertain significance |
| rs1335010586 | 4:106,580,341 | C/T | — | uncertain significance |
| rs904369371 | 4:106,580,356 | A/T | — | uncertain significance |
| rs553330310 | 4:106,580,373 | T/A | — | uncertain significance |
| rs1460548015 | 4:106,580,387 | C/A | — | uncertain significance |
| rs762706521 | 4:106,580,427 | G/A | — | uncertain significance |
| rs2476504296 | 4:106,587,377 | T/G | — | uncertain significance |
| rs868324600 | 4:106,587,421 | G/A | — | uncertain significance |
| rs2476507184 | 4:106,588,400 | A/C | — | uncertain significance |
| rs1002069630 | 4:106,588,640 | A/G | — | uncertain significance |
| rs2476508195 | 4:106,588,670 | C/G | — | uncertain significance |
| rs2476508279 | 4:106,588,684 | T/C | — | uncertain significance |
| rs778608312 | 4:106,588,690 | G/A | — | uncertain significance |
| rs767209283 | 4:106,588,727 | G/A | — | uncertain significance |
| rs115599607 | 4:106,590,294 | T/C | — | — |
| rs1180347761 | 4:106,598,943 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.