BPIFB3
BPI fold containing family B member 3
Summary
Predicted to enable lipid binding activity. Predicted to be involved in innate immune response. Located in cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants31 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs127896 | 20:31,641,290 | G/C | — | — |
| rs144150108 | 20:31,643,322 | C/T | — | likely benign |
| rs138919082 | 20:31,643,323 | G/T | — | uncertain significance |
| rs779603595 | 20:31,644,372 | A/G | — | likely benign |
| rs150025342 | 20:31,644,410 | G/A | — | uncertain significance |
| rs765820847 | 20:31,644,438 | G/A | — | uncertain significance |
| rs749297272 | 20:31,644,470 | G/C | — | uncertain significance |
| rs146748300 | 20:31,646,479 | T/G | upstream gene variant | — |
| rs761108841 | 20:31,647,204 | C/T | — | uncertain significance |
| rs2516039459 | 20:31,647,723 | C/T | — | uncertain significance |
| rs781712029 | 20:31,647,747 | G/A | — | uncertain significance |
| rs376567897 | 20:31,647,773 | G/A | — | uncertain significance |
| rs149445561 | 20:31,647,807 | C/G | — | uncertain significance |
| rs780356284 | 20:31,647,816 | G/A | — | uncertain significance |
| rs2516042455 | 20:31,649,614 | C/G | — | uncertain significance |
| rs752568270 | 20:31,652,338 | T/C | — | uncertain significance |
| rs143149440 | 20:31,652,507 | C/A | — | uncertain significance |
| rs201111989 | 20:31,652,538 | C/T | — | uncertain significance |
| rs922686856 | 20:31,652,631 | A/C | — | uncertain significance |
| rs768724368 | 20:31,652,643 | C/A | — | uncertain significance |
| rs148332356 | 20:31,655,763 | T/C | intron variant | — |
| rs765474556 | 20:31,656,688 | A/G | — | uncertain significance |
| rs142099629 | 20:31,656,690 | A/G | — | uncertain significance |
| rs201582304 | 20:31,656,697 | C/A | — | uncertain significance |
| rs2516052893 | 20:31,656,744 | A/G | — | uncertain significance |
| rs1980776415 | 20:31,656,767 | T/G | — | uncertain significance |
| rs41289874 | 20:31,657,658 | G/C | intron variant | — |
| rs151032238 | 20:31,657,752 | C/A | — | uncertain significance |
| rs140066843 | 20:31,660,525 | G/A | — | uncertain significance |
| rs754962643 | 20:31,660,531 | G/A | — | uncertain significance |
| rs767999839 | 20:31,660,592 | T/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.