A1BG
alpha-1-B glycoprotein
Summary
The protein encoded by this gene is a plasma glycoprotein of unknown function. The protein shows sequence similarity to the variable regions of some immunoglobulin supergene family member proteins. [provided by RefSeq, Jul 2008]
Known Variants44 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1326085462 | 19:58,858,736 | A/T | — | uncertain significance |
| rs774591364 | 19:58,858,782 | G/C | — | uncertain significance |
| rs995585388 | 19:58,858,854 | G/C | — | uncertain significance |
| rs2051922254 | 19:58,858,860 | G/A | — | uncertain significance |
| rs757030081 | 19:58,858,882 | C/G | — | uncertain significance |
| rs755735308 | 19:58,858,888 | C/G | — | uncertain significance |
| rs776948818 | 19:58,858,923 | G/A | — | uncertain significance |
| rs778239053 | 19:58,858,982 | C/T | — | uncertain significance |
| rs902106978 | 19:58,861,805 | C/T | — | uncertain significance |
| rs145144275 | 19:58,861,808 | A/G | — | likely benign |
| rs2051947306 | 19:58,861,822 | G/A | — | uncertain significance |
| rs1433781988 | 19:58,861,858 | G/T | — | uncertain significance |
| rs145513899 | 19:58,861,859 | C/T | — | uncertain significance |
| rs919150156 | 19:58,861,908 | G/C | — | uncertain significance |
| rs756511381 | 19:58,861,921 | A/C | — | uncertain significance |
| rs1426741918 | 19:58,861,925 | C/T | — | uncertain significance |
| rs1568553352 | 19:58,861,930 | C/G | — | uncertain significance |
| rs1439769564 | 19:58,861,937 | C/A | — | uncertain significance |
| rs1263342364 | 19:58,861,940 | C/T | — | uncertain significance |
| rs1305665724 | 19:58,861,976 | C/T | — | uncertain significance |
| rs1038758891 | 19:58,861,990 | G/A | — | uncertain significance |
| rs922976117 | 19:58,862,005 | G/T | — | uncertain significance |
| rs149231769 | 19:58,862,783 | G/A | — | uncertain significance |
| rs143384169 | 19:58,862,790 | C/T | — | uncertain significance |
| rs375770905 | 19:58,862,834 | G/T | — | uncertain significance |
| rs2516635840 | 19:58,862,849 | T/C | — | uncertain significance |
| rs930140223 | 19:58,862,925 | T/G | — | uncertain significance |
| rs200002683 | 19:58,862,931 | C/T | — | uncertain significance |
| rs752473132 | 19:58,862,964 | G/T | — | uncertain significance |
| rs200922339 | 19:58,863,658 | C/T | — | likely benign |
| rs374704838 | 19:58,863,734 | C/G | — | uncertain significance |
| rs892699925 | 19:58,863,747 | A/G | — | uncertain significance |
| rs2516637902 | 19:58,863,782 | C/G | — | uncertain significance |
| rs769410420 | 19:58,863,807 | C/T | — | uncertain significance |
| rs372209543 | 19:58,863,831 | C/T | — | uncertain significance |
| rs1404927822 | 19:58,863,865 | G/C | — | uncertain significance |
| rs372876362 | 19:58,863,870 | G/T | — | uncertain significance |
| rs527636153 | 19:58,864,329 | G/C | — | uncertain significance |
| rs2516639732 | 19:58,864,374 | G/A | — | uncertain significance |
| rs747803919 | 19:58,864,386 | A/T | — | uncertain significance |
| rs534286441 | 19:58,864,430 | C/A | — | uncertain significance |
| rs2516640002 | 19:58,864,460 | G/T | — | uncertain significance |
| rs893184 | 19:58,864,479 | T/C | missense variant | — |
| rs7256067 | 19:58,864,491 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.