ARRDC2
arrestin domain containing 2
Summary
Predicted to be involved in protein transport. Located in cytoplasmic vesicle and plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants29 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs530160304 | 19:18,112,128 | G/A | — | uncertain significance |
| rs1045114947 | 19:18,112,151 | G/C | — | uncertain significance |
| rs35928002 | 19:18,116,144 | A/G | regulatory region variant | — |
| rs771782546 | 19:18,119,183 | C/T | — | uncertain significance |
| rs758085197 | 19:18,119,217 | G/A | — | uncertain significance |
| rs202031500 | 19:18,119,313 | C/G | — | uncertain significance |
| rs780715164 | 19:18,119,820 | C/A | — | uncertain significance |
| rs756733526 | 19:18,119,878 | A/G | — | uncertain significance |
| rs1009744292 | 19:18,120,435 | G/A | — | uncertain significance |
| rs757352581 | 19:18,120,471 | C/T | — | uncertain significance |
| rs1214758605 | 19:18,120,482 | G/A | — | uncertain significance |
| rs148747793 | 19:18,120,485 | C/T | — | uncertain significance |
| rs1268182483 | 19:18,120,616 | A/G | — | uncertain significance |
| rs774002258 | 19:18,120,694 | C/T | — | uncertain significance |
| rs368207032 | 19:18,120,741 | G/C | — | uncertain significance |
| rs763115592 | 19:18,120,774 | C/T | — | uncertain significance |
| rs2514804539 | 19:18,120,777 | G/A | — | uncertain significance |
| rs529559915 | 19:18,120,783 | C/T | — | uncertain significance |
| rs115826747 | 19:18,120,784 | G/A | — | uncertain significance |
| rs752261569 | 19:18,120,795 | G/A | — | uncertain significance |
| rs2033386336 | 19:18,121,152 | C/A | — | uncertain significance |
| rs2033393338 | 19:18,121,458 | G/A | — | uncertain significance |
| rs2033393387 | 19:18,121,461 | C/G | — | uncertain significance |
| rs369066496 | 19:18,121,510 | G/A | — | uncertain significance |
| rs537634477 | 19:18,121,519 | C/T | — | uncertain significance |
| rs762156413 | 19:18,121,522 | C/T | — | uncertain significance |
| rs772523798 | 19:18,121,525 | C/T | — | uncertain significance |
| rs8104679 | 19:18,121,967 | T/C | intron variant | — |
| rs1298060052 | 19:18,123,756 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.