ARHGEF37
Rho guanine nucleotide exchange factor 37
Summary
Predicted to enable guanyl-nucleotide exchange factor activity. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants47 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs138543916 | 5:148,945,475 | C/T | regulatory region variant | — |
| rs1763592357 | 5:148,977,409 | G/A | — | likely benign |
| rs748814270 | 5:148,977,412 | C/T | — | uncertain significance |
| rs774059450 | 5:148,977,420 | C/T | — | uncertain significance |
| rs199767707 | 5:148,977,433 | C/G | — | uncertain significance |
| rs761050803 | 5:148,977,444 | C/T | — | uncertain significance |
| rs200527896 | 5:148,977,507 | C/T | — | uncertain significance |
| rs200052393 | 5:148,980,675 | C/T | — | uncertain significance |
| rs373387739 | 5:148,980,680 | G/A | — | uncertain significance |
| rs751208682 | 5:148,980,767 | A/C | — | uncertain significance |
| rs745962223 | 5:148,989,116 | A/G | — | uncertain significance |
| rs1764020510 | 5:148,989,218 | G/A | — | uncertain significance |
| rs749111091 | 5:148,989,221 | C/G | — | uncertain significance |
| rs374655369 | 5:148,996,317 | C/T | — | uncertain significance |
| rs547194661 | 5:148,996,318 | G/A | — | uncertain significance |
| rs1184681238 | 5:148,997,749 | C/T | — | likely benign |
| rs778497862 | 5:148,997,756 | G/A | — | uncertain significance |
| rs372222488 | 5:148,997,825 | C/T | — | uncertain significance |
| rs777474731 | 5:148,997,859 | T/G | — | uncertain significance |
| rs753545664 | 5:148,998,510 | A/G | — | uncertain significance |
| rs1404405373 | 5:148,998,514 | A/G | — | uncertain significance |
| rs368910887 | 5:148,999,940 | C/T | — | likely benign |
| rs1752504161 | 5:148,999,944 | T/C | — | uncertain significance |
| rs755177143 | 5:149,000,005 | A/C | — | uncertain significance |
| rs758292615 | 5:149,001,308 | G/A | — | uncertain significance |
| rs2479769110 | 5:149,001,351 | T/C | — | uncertain significance |
| rs372019080 | 5:149,001,381 | G/A | — | uncertain significance |
| rs2479769584 | 5:149,001,420 | A/G | — | uncertain significance |
| rs1220017488 | 5:149,001,479 | G/C | — | uncertain significance |
| rs776755385 | 5:149,001,562 | C/G | — | uncertain significance |
| rs180816699 | 5:149,001,567 | C/T | — | uncertain significance |
| rs200707149 | 5:149,001,592 | A/C | — | uncertain significance |
| rs775287566 | 5:149,003,639 | C/T | — | uncertain significance |
| rs1158915440 | 5:149,003,699 | C/T | — | uncertain significance |
| rs767741283 | 5:149,006,660 | C/T | — | uncertain significance |
| rs780868133 | 5:149,006,711 | G/A | — | uncertain significance |
| rs758558572 | 5:149,006,775 | C/G | — | uncertain significance |
| rs373710218 | 5:149,006,796 | C/G | — | uncertain significance |
| rs764425139 | 5:149,006,829 | C/G | — | uncertain significance |
| rs543805061 | 5:149,008,376 | T/A | — | uncertain significance |
| rs377386792 | 5:149,008,423 | C/G | — | uncertain significance |
| rs759749530 | 5:149,008,471 | G/A | — | uncertain significance |
| rs752099085 | 5:149,008,525 | A/T | — | uncertain significance |
| rs183228970 | 5:149,009,622 | G/C | intron variant | — |
| rs776949148 | 5:149,011,555 | C/T | — | likely benign |
| rs201695271 | 5:149,011,556 | G/A | — | likely benign |
| rs2479808164 | 5:149,011,567 | T/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.