ARHGEF16
Rho guanine nucleotide exchange factor 16
Summary
Although the specific function of this protein is not known yet, it is thought to be involved in protein-protein and protein-lipid interactions. [provided by RefSeq, Jul 2008]
Known Variants66 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs143540794 | 1:3,376,898 | G/A | regulatory region variant | — |
| rs1045272383 | 1:3,379,659 | G/A | — | uncertain significance |
| rs942176075 | 1:3,379,700 | C/T | — | uncertain significance |
| rs1038152955 | 1:3,379,701 | G/A | — | uncertain significance |
| rs547639596 | 1:3,379,733 | G/C | — | uncertain significance |
| rs751723822 | 1:3,379,764 | G/A | — | uncertain significance |
| rs556522799 | 1:3,379,889 | C/G | — | uncertain significance |
| rs1639453206 | 1:3,379,944 | C/T | — | uncertain significance |
| rs541615611 | 1:3,380,003 | C/T | — | uncertain significance |
| rs550096684 | 1:3,380,040 | C/A | — | uncertain significance |
| rs777253808 | 1:3,380,072 | G/A | — | uncertain significance |
| rs1453195678 | 1:3,380,111 | C/T | — | uncertain significance |
| rs1031473979 | 1:3,380,112 | G/A | — | uncertain significance |
| rs187419731 | 1:3,380,217 | G/A | — | uncertain significance |
| rs924346370 | 1:3,383,806 | G/A | — | uncertain significance |
| rs775696698 | 1:3,383,816 | G/C | — | uncertain significance |
| rs894088724 | 1:3,383,861 | G/C | — | uncertain significance |
| rs1462238873 | 1:3,383,866 | C/T | — | uncertain significance |
| rs1012460755 | 1:3,383,867 | G/A | — | uncertain significance |
| rs1267008760 | 1:3,385,450 | G/A | — | uncertain significance |
| rs760221421 | 1:3,385,481 | A/G | — | uncertain significance |
| rs776340254 | 1:3,386,001 | T/C | — | uncertain significance |
| rs1639641960 | 1:3,386,006 | G/A | — | uncertain significance |
| rs199607431 | 1:3,386,019 | C/T | — | uncertain significance |
| rs1639643574 | 1:3,386,028 | C/T | — | uncertain significance |
| rs778961636 | 1:3,386,045 | A/G | — | likely benign |
| rs138148473 | 1:3,386,054 | G/A | — | uncertain significance |
| rs140093908 | 1:3,386,084 | C/T | — | uncertain significance |
| rs1048897523 | 1:3,386,085 | G/T | — | uncertain significance |
| rs35754076 | 1:3,386,089 | G/A | — | benign |
| rs776606730 | 1:3,389,649 | G/C | — | uncertain significance |
| rs1428821464 | 1:3,389,664 | C/T | — | uncertain significance |
| rs536938385 | 1:3,389,665 | G/A | — | uncertain significance |
| rs141425462 | 1:3,389,703 | A/G | — | uncertain significance |
| rs147324873 | 1:3,389,718 | G/T | — | uncertain significance |
| rs2521695631 | 1:3,389,721 | G/C | — | uncertain significance |
| rs41315284 | 1:3,389,757 | A/G | missense variant | — |
| rs774950266 | 1:3,389,974 | T/C | — | uncertain significance |
| rs1209365753 | 1:3,389,977 | G/A | — | uncertain significance |
| rs1639795771 | 1:3,390,028 | T/C | — | uncertain significance |
| rs750937556 | 1:3,391,344 | A/C | — | uncertain significance |
| rs2521713543 | 1:3,392,543 | C/A | — | uncertain significance |
| rs2521714313 | 1:3,392,585 | A/T | — | uncertain significance |
| rs201584820 | 1:3,392,588 | T/C | — | uncertain significance |
| rs777092820 | 1:3,394,442 | C/T | — | uncertain significance |
| rs756061209 | 1:3,394,461 | C/G | — | uncertain significance |
| rs747219652 | 1:3,394,518 | G/A | — | uncertain significance |
| rs373186673 | 1:3,394,562 | G/A | — | uncertain significance |
| rs567294084 | 1:3,394,571 | G/T | — | uncertain significance |
| rs74050529 | 1:3,395,002 | T/C | — | benign |
| rs201085717 | 1:3,395,038 | T/A | — | uncertain significance |
| rs1489788224 | 1:3,395,061 | C/A | — | uncertain significance |
| rs749083124 | 1:3,395,065 | C/A | — | uncertain significance |
| rs143167978 | 1:3,395,085 | C/T | — | uncertain significance |
| rs139024357 | 1:3,395,097 | G/A | — | likely benign |
| rs201282947 | 1:3,395,113 | A/G | — | uncertain significance |
| rs759695331 | 1:3,395,145 | C/G | — | uncertain significance |
| rs1639963488 | 1:3,395,152 | A/G | — | uncertain significance |
| rs1164678933 | 1:3,396,104 | T/C | — | uncertain significance |
| rs2521742875 | 1:3,396,143 | C/G | — | uncertain significance |
| rs77854264 | 1:3,396,163 | G/A | — | benign |
| rs180731913 | 1:3,396,412 | C/T | — | uncertain significance |
| rs1640025714 | 1:3,397,039 | A/T | — | uncertain significance |
| rs186738663 | 1:3,397,041 | G/A | — | uncertain significance |
| rs534395921 | 1:3,397,075 | G/A | — | uncertain significance |
| rs1385359729 | 1:3,397,080 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.