ARHGAP39
Rho GTPase activating protein 39
Summary
Predicted to enable GTPase activator activity. Involved in postsynapse organization. Is active in glutamatergic synapse. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants83 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs752943391 | 8:145,755,895 | C/T | — | uncertain significance |
| rs1486803757 | 8:145,755,972 | A/G | — | uncertain significance |
| rs1464653412 | 8:145,756,096 | C/T | — | uncertain significance |
| rs771986069 | 8:145,756,108 | C/G | — | uncertain significance |
| rs369823775 | 8:145,756,120 | C/T | — | uncertain significance |
| rs748339987 | 8:145,756,193 | C/T | — | uncertain significance |
| rs371456040 | 8:145,758,634 | C/T | — | uncertain significance |
| rs759866316 | 8:145,758,679 | G/A | — | uncertain significance |
| rs1459473413 | 8:145,759,553 | T/C | — | uncertain significance |
| rs1564835517 | 8:145,763,161 | G/C | — | likely benign |
| rs61748959 | 8:145,770,700 | G/A | — | benign |
| rs752652890 | 8:145,770,746 | C/A | — | uncertain significance |
| rs2538271518 | 8:145,770,774 | C/T | — | uncertain significance |
| rs147513432 | 8:145,770,818 | C/G | — | uncertain significance |
| rs375868923 | 8:145,770,825 | C/T | — | uncertain significance |
| rs1817385383 | 8:145,771,055 | T/C | — | uncertain significance |
| rs747197911 | 8:145,771,124 | C/T | — | uncertain significance |
| rs757366577 | 8:145,771,137 | C/T | — | likely benign |
| rs751149248 | 8:145,771,143 | T/C | — | uncertain significance |
| rs11994207 | 8:145,771,154 | C/T | missense variant | — |
| rs557229440 | 8:145,771,164 | C/T | — | uncertain significance |
| rs1177682286 | 8:145,771,169 | T/C | — | uncertain significance |
| rs2538276137 | 8:145,772,527 | T/C | — | uncertain significance |
| rs200560505 | 8:145,772,587 | G/C | — | uncertain significance |
| rs2538276899 | 8:145,772,696 | G/A | — | uncertain significance |
| rs201556048 | 8:145,772,828 | C/T | — | uncertain significance |
| rs2538277576 | 8:145,772,836 | C/T | — | uncertain significance |
| rs751091820 | 8:145,772,857 | C/T | — | uncertain significance |
| rs760609039 | 8:145,772,891 | G/A | — | uncertain significance |
| rs762118130 | 8:145,772,932 | G/A | — | uncertain significance |
| rs1454909970 | 8:145,772,936 | C/T | — | uncertain significance |
| rs777563207 | 8:145,772,995 | C/T | — | uncertain significance |
| rs1394532233 | 8:145,772,998 | G/C | — | uncertain significance |
| rs754308674 | 8:145,773,034 | T/C | — | uncertain significance |
| rs556385108 | 8:145,773,061 | T/C | — | uncertain significance |
| rs745752310 | 8:145,773,088 | G/A | — | uncertain significance |
| rs1817507727 | 8:145,773,109 | G/A | — | uncertain significance |
| rs1192627282 | 8:145,773,139 | T/C | — | likely benign |
| rs1299581498 | 8:145,773,142 | A/G | — | uncertain significance |
| rs1265422797 | 8:145,773,158 | C/A | — | uncertain significance |
| rs2130844427 | 8:145,773,215 | C/G | — | uncertain significance |
| rs750579993 | 8:145,773,226 | C/T | — | uncertain significance |
| rs1048385275 | 8:145,773,238 | C/A | — | uncertain significance |
| rs1180772327 | 8:145,773,265 | T/C | — | uncertain significance |
| rs1346234374 | 8:145,773,283 | C/T | — | uncertain significance |
| rs768217425 | 8:145,773,331 | T/C | — | uncertain significance |
| rs1340218354 | 8:145,773,340 | T/G | — | uncertain significance |
| rs778151738 | 8:145,773,377 | G/T | — | uncertain significance |
| rs371369532 | 8:145,773,413 | G/A | — | uncertain significance |
| rs367945395 | 8:145,773,430 | C/T | — | uncertain significance |
| rs151220486 | 8:145,773,436 | G/A | — | uncertain significance |
| rs748621226 | 8:145,773,475 | A/G | — | uncertain significance |
| rs759287973 | 8:145,773,505 | G/T | — | uncertain significance |
| rs769537433 | 8:145,773,506 | C/T | — | uncertain significance |
| rs201484808 | 8:145,773,539 | G/C | — | uncertain significance |
| rs375834942 | 8:145,773,541 | G/C | — | uncertain significance |
| rs778326683 | 8:145,773,542 | G/T | — | uncertain significance |
| rs369269697 | 8:145,773,556 | C/T | — | uncertain significance |
| rs765548488 | 8:145,773,595 | G/A | — | uncertain significance |
| rs763440661 | 8:145,773,674 | A/T | — | uncertain significance |
| rs1054600136 | 8:145,773,727 | C/G | — | uncertain significance |
| rs769951591 | 8:145,773,749 | G/C | — | uncertain significance |
| rs139206529 | 8:145,773,764 | C/T | — | likely benign |
| rs61734939 | 8:145,773,789 | G/C | — | benign |
| rs1817567506 | 8:145,773,831 | C/T | — | uncertain significance |
| rs2620636 | 8:145,778,128 | C/T | downstream gene variant | — |
| rs948668753 | 8:145,780,980 | C/T | — | uncertain significance |
| rs544983952 | 8:145,780,999 | T/C | — | uncertain significance |
| rs200627287 | 8:145,806,284 | G/A | — | uncertain significance |
| rs376803658 | 8:145,806,347 | C/A | — | uncertain significance |
| rs759404928 | 8:145,806,353 | A/C | — | uncertain significance |
| rs765156214 | 8:145,806,360 | T/C | — | uncertain significance |
| rs369803124 | 8:145,806,383 | G/A | — | uncertain significance |
| rs777316055 | 8:145,806,491 | T/C | — | likely benign |
| rs369204996 | 8:145,806,620 | C/T | — | uncertain significance |
| rs572851824 | 8:145,806,661 | C/G | — | likely benign |
| rs367748801 | 8:145,830,943 | C/T | — | likely benign |
| rs200377993 | 8:145,830,957 | C/G | — | uncertain significance |
| rs540971103 | 8:145,830,975 | A/G | — | uncertain significance |
| rs150289481 | 8:145,830,989 | G/C | — | uncertain significance |
| rs117889339 | 8:145,840,377 | C/T | intron variant | — |
| rs138190448 | 8:145,878,521 | A/G | intron variant | — |
| rs12719778 | 8:145,879,883 | T/C | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.