RFTN2
raftlin family member 2
Summary
Predicted to act upstream of or within dsRNA transport and response to exogenous dsRNA. Predicted to be located in plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants32 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2468699319 | 2:198,436,757 | C/G | — | uncertain significance |
| rs752094547 | 2:198,436,800 | C/T | — | uncertain significance |
| rs1224658489 | 2:198,436,829 | C/A | — | uncertain significance |
| rs1309468241 | 2:198,436,831 | G/C | — | uncertain significance |
| rs527815128 | 2:198,436,836 | G/A | — | likely benign |
| rs115896530 | 2:198,436,886 | C/T | — | uncertain significance |
| rs139202328 | 2:198,436,934 | G/A | — | uncertain significance |
| rs775817578 | 2:198,436,955 | C/T | — | uncertain significance |
| rs2468700644 | 2:198,436,989 | G/A | — | uncertain significance |
| rs768206974 | 2:198,436,992 | G/A | — | uncertain significance |
| rs6715105 | 2:198,445,601 | T/C | intron variant | — |
| rs750187644 | 2:198,460,742 | C/T | — | uncertain significance |
| rs199832032 | 2:198,460,765 | C/T | — | uncertain significance |
| rs116386838 | 2:198,472,334 | C/T | intron variant | — |
| rs542147954 | 2:198,480,609 | C/G | — | uncertain significance |
| rs146246670 | 2:198,480,625 | G/C | — | uncertain significance |
| rs776572146 | 2:198,482,640 | G/A | — | uncertain significance |
| rs1902247 | 2:198,492,826 | C/T | regulatory region variant | — |
| rs2468838374 | 2:198,498,466 | A/G | — | uncertain significance |
| rs764624297 | 2:198,498,511 | G/T | — | uncertain significance |
| rs2468838737 | 2:198,498,524 | C/G | — | uncertain significance |
| rs1186682633 | 2:198,498,610 | G/C | — | uncertain significance |
| rs756237903 | 2:198,498,715 | C/T | — | uncertain significance |
| rs1184758656 | 2:198,508,946 | A/T | — | uncertain significance |
| rs532034102 | 2:198,508,961 | C/T | — | uncertain significance |
| rs375521440 | 2:198,508,980 | C/A | — | uncertain significance |
| rs758499071 | 2:198,508,996 | G/C | — | uncertain significance |
| rs765379863 | 2:198,511,219 | C/T | — | uncertain significance |
| rs2088754126 | 2:198,511,348 | T/C | — | uncertain significance |
| rs6733834 | 2:198,518,709 | C/T | — | — |
| rs6757852 | 2:198,530,293 | G/T | — | — |
| rs77946222 | 2:198,533,251 | C/T | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.