ENDOD1
endonuclease domain containing 1
Summary
Predicted to enable endonuclease activity; metal ion binding activity; and nucleic acid binding activity. Predicted to be involved in innate immune response. Located in extracellular exosome and membrane. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants33 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs773581617 | 11:94,823,108 | G/C | — | uncertain significance |
| rs868994321 | 11:94,823,125 | C/T | — | uncertain significance |
| rs369404308 | 11:94,823,195 | A/T | — | uncertain significance |
| rs782473706 | 11:94,823,224 | G/T | — | uncertain significance |
| rs539609900 | 11:94,823,321 | T/G | — | uncertain significance |
| rs558314943 | 11:94,823,329 | G/A | — | uncertain significance |
| rs1858914148 | 11:94,823,338 | G/T | — | uncertain significance |
| rs2496581075 | 11:94,823,344 | C/T | — | uncertain significance |
| rs367564707 | 11:94,823,359 | G/T | — | uncertain significance |
| rs641937 | 11:94,833,022 | C/G | intron variant | — |
| rs965080410 | 11:94,861,618 | C/A | — | uncertain significance |
| rs184192678 | 11:94,861,636 | A/G | — | likely benign |
| rs200694967 | 11:94,861,757 | C/T | — | uncertain significance |
| rs771483722 | 11:94,861,787 | G/A | — | uncertain significance |
| rs184606168 | 11:94,861,846 | A/G | — | likely benign |
| rs1159796904 | 11:94,861,868 | A/G | — | uncertain significance |
| rs923134732 | 11:94,861,874 | A/G | — | uncertain significance |
| rs2496626825 | 11:94,861,950 | T/A | — | uncertain significance |
| rs200529219 | 11:94,861,961 | C/T | — | uncertain significance |
| rs374060470 | 11:94,861,962 | G/A | — | likely benign |
| rs1421308261 | 11:94,862,066 | A/C | — | uncertain significance |
| rs2496627134 | 11:94,862,076 | T/C | — | uncertain significance |
| rs527831603 | 11:94,862,091 | A/C | — | uncertain significance |
| rs184092436 | 11:94,862,234 | A/G | — | uncertain significance |
| rs1565450141 | 11:94,862,264 | C/T | — | uncertain significance |
| rs551599857 | 11:94,862,280 | A/T | — | uncertain significance |
| rs776689266 | 11:94,862,295 | C/A | — | uncertain significance |
| rs61740357 | 11:94,862,328 | G/A | — | likely benign |
| rs754879387 | 11:94,862,355 | T/C | — | uncertain significance |
| rs2496627764 | 11:94,862,367 | T/G | — | uncertain significance |
| rs1023299886 | 11:94,862,390 | A/G | — | likely benign |
| rs181056490 | 11:94,862,453 | G/A | — | likely benign |
| rs202063615 | 11:94,862,552 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.