XRRA1
X-ray radiation resistance associated 1
Summary
Involved in response to X-ray. Located in cytoplasm and nuclear body. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants60 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1479087823 | 11:74,554,286 | C/T | — | uncertain significance |
| rs2547391664 | 11:74,554,341 | G/C | — | uncertain significance |
| rs1565202953 | 11:74,554,361 | T/C | — | uncertain significance |
| rs891011539 | 11:74,554,367 | C/T | — | likely benign |
| rs372121351 | 11:74,554,374 | T/C | — | likely benign |
| rs753120857 | 11:74,554,402 | C/T | — | uncertain significance |
| rs758982331 | 11:74,554,403 | G/A | — | uncertain significance |
| rs769692770 | 11:74,554,416 | G/C | — | uncertain significance |
| rs1260114124 | 11:74,554,421 | C/T | — | uncertain significance |
| rs758776602 | 11:74,554,493 | C/T | — | uncertain significance |
| rs757402365 | 11:74,554,498 | C/T | — | uncertain significance |
| rs113420599 | 11:74,554,922 | C/A | — | uncertain significance |
| rs2547415552 | 11:74,554,930 | C/A | — | likely benign |
| rs199764887 | 11:74,554,933 | C/A | — | uncertain significance |
| rs768149411 | 11:74,554,937 | C/T | — | uncertain significance |
| rs2547415822 | 11:74,554,939 | A/C | — | uncertain significance |
| rs777684962 | 11:74,554,991 | G/C | — | uncertain significance |
| rs747007037 | 11:74,554,999 | C/G | — | uncertain significance |
| rs775669740 | 11:74,555,232 | T/C | — | uncertain significance |
| rs1476978101 | 11:74,555,289 | T/C | — | uncertain significance |
| rs760550620 | 11:74,556,294 | A/G | — | uncertain significance |
| rs1275501756 | 11:74,556,312 | C/G | — | uncertain significance |
| rs776601021 | 11:74,559,183 | T/G | — | uncertain significance |
| rs745752535 | 11:74,559,188 | T/C | — | uncertain significance |
| rs144693538 | 11:74,559,209 | C/T | — | likely benign |
| rs761489735 | 11:74,559,225 | G/A | — | uncertain significance |
| rs768167272 | 11:74,559,254 | G/A | — | uncertain significance |
| rs2038820025 | 11:74,559,294 | G/T | — | uncertain significance |
| rs371407553 | 11:74,559,312 | G/A | — | uncertain significance |
| rs370758327 | 11:74,559,329 | C/T | — | uncertain significance |
| rs914067118 | 11:74,559,333 | C/G | — | uncertain significance |
| rs771635204 | 11:74,559,384 | G/T | — | uncertain significance |
| rs200117660 | 11:74,562,138 | A/G | — | likely benign |
| rs368010821 | 11:74,562,156 | T/G | — | uncertain significance |
| rs748531166 | 11:74,562,176 | T/C | — | uncertain significance |
| rs370520559 | 11:74,562,182 | A/G | — | likely benign |
| rs747601755 | 11:74,562,196 | T/G | — | uncertain significance |
| rs746397444 | 11:74,563,058 | T/G | — | uncertain significance |
| rs375219655 | 11:74,563,124 | C/T | — | uncertain significance |
| rs749394019 | 11:74,570,288 | A/T | — | uncertain significance |
| rs1200054342 | 11:74,570,309 | A/C | — | uncertain significance |
| rs201462193 | 11:74,570,320 | C/G | — | uncertain significance |
| rs780878723 | 11:74,617,290 | G/A | — | uncertain significance |
| rs1186931187 | 11:74,617,314 | G/T | — | uncertain significance |
| rs1422998576 | 11:74,617,407 | C/T | — | uncertain significance |
| rs201475280 | 11:74,618,208 | C/T | — | uncertain significance |
| rs533441391 | 11:74,618,223 | G/A | — | uncertain significance |
| rs757814270 | 11:74,618,286 | C/G | — | uncertain significance |
| rs1372035131 | 11:74,618,289 | T/C | — | uncertain significance |
| rs762731078 | 11:74,632,277 | T/C | — | uncertain significance |
| rs949138724 | 11:74,632,370 | C/T | — | uncertain significance |
| rs2548913496 | 11:74,632,385 | T/C | — | uncertain significance |
| rs780026133 | 11:74,638,492 | C/T | — | uncertain significance |
| rs909412990 | 11:74,641,356 | A/C | — | uncertain significance |
| rs199520391 | 11:74,647,981 | C/A | — | uncertain significance |
| rs201171442 | 11:74,647,982 | G/A | — | uncertain significance |
| rs202056915 | 11:74,648,036 | G/A | — | uncertain significance |
| rs200911624 | 11:74,648,062 | T/C | — | likely benign |
| rs1945167553 | 11:74,648,104 | T/C | — | uncertain significance |
| rs193143010 | 11:74,656,658 | C/T | upstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.