EXD1
exonuclease 3'-5' domain containing 1
Summary
Predicted to enable RNA binding activity and protein homodimerization activity. Predicted to be involved in piRNA processing. Predicted to be located in P granule. Predicted to be part of PET complex. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants35 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2543058156 | 15:41,476,168 | C/A | — | uncertain significance |
| rs761206209 | 15:41,476,178 | G/C | — | uncertain significance |
| rs764657350 | 15:41,476,272 | T/C | — | likely benign |
| rs185697361 | 15:41,476,287 | T/C | — | uncertain significance |
| rs369400894 | 15:41,476,332 | C/T | — | uncertain significance |
| rs756077141 | 15:41,476,336 | C/A | — | uncertain significance |
| rs374548709 | 15:41,476,470 | C/T | — | uncertain significance |
| rs755130305 | 15:41,476,604 | C/G | — | uncertain significance |
| rs372898407 | 15:41,476,670 | A/G | — | uncertain significance |
| rs377668115 | 15:41,476,744 | G/C | — | uncertain significance |
| rs758861605 | 15:41,482,139 | G/A | — | uncertain significance |
| rs2046479191 | 15:41,482,149 | G/A | — | uncertain significance |
| rs771880504 | 15:41,482,169 | C/T | — | uncertain significance |
| rs1372676201 | 15:41,482,194 | C/T | — | uncertain significance |
| rs748905860 | 15:41,482,239 | G/A | — | uncertain significance |
| rs777874912 | 15:41,482,263 | C/T | — | uncertain significance |
| rs760453190 | 15:41,482,268 | G/A | — | uncertain significance |
| rs763620121 | 15:41,482,301 | C/T | — | uncertain significance |
| rs377220541 | 15:41,482,314 | C/A | — | uncertain significance |
| rs2543094194 | 15:41,483,643 | A/C | — | uncertain significance |
| rs1289065178 | 15:41,483,656 | C/T | — | uncertain significance |
| rs761035017 | 15:41,483,716 | T/G | — | uncertain significance |
| rs138628477 | 15:41,483,723 | T/C | — | uncertain significance |
| rs756099101 | 15:41,483,749 | C/T | — | uncertain significance |
| rs200349978 | 15:41,483,752 | G/A | — | uncertain significance |
| rs146356287 | 15:41,483,783 | C/T | — | uncertain significance |
| rs2046602415 | 15:41,488,023 | A/G | — | uncertain significance |
| rs1453139021 | 15:41,488,172 | T/C | — | uncertain significance |
| rs8039934 | 15:41,497,427 | T/C | intron variant | — |
| rs764879151 | 15:41,508,908 | G/A | — | uncertain significance |
| rs201884910 | 15:41,508,919 | G/T | — | uncertain significance |
| rs757382690 | 15:41,508,963 | T/G | — | uncertain significance |
| rs2543185032 | 15:41,509,304 | G/C | — | uncertain significance |
| rs565470172 | 15:41,514,971 | A/T | — | — |
| rs772980179 | 15:41,522,694 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.