BPIFB4
BPI fold containing family B member 4
Summary
Predicted to enable lipid binding activity. Located in actin cytoskeleton and cytosol. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants40 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs752760419 | 20:31,669,358 | C/T | — | uncertain significance |
| rs1439551576 | 20:31,669,404 | G/A | — | likely benign |
| rs767145060 | 20:31,669,408 | C/A | — | uncertain significance |
| rs190967709 | 20:31,669,812 | A/G | intron variant | — |
| rs979395810 | 20:31,670,913 | T/G | — | likely benign |
| rs1453647973 | 20:31,671,019 | T/C | — | likely benign |
| rs144580332 | 20:31,671,181 | G/A | — | uncertain significance |
| rs370732161 | 20:31,671,220 | C/G | — | uncertain significance |
| rs150980536 | 20:31,671,221 | C/A | — | uncertain significance |
| rs2516071176 | 20:31,671,251 | G/A | — | uncertain significance |
| rs2516071276 | 20:31,671,292 | G/T | — | uncertain significance |
| rs779799200 | 20:31,671,302 | G/C | — | uncertain significance |
| rs781326746 | 20:31,671,337 | G/A | — | uncertain significance |
| rs1166194271 | 20:31,671,479 | C/A | — | uncertain significance |
| rs955403549 | 20:31,671,533 | T/C | — | uncertain significance |
| rs2516071888 | 20:31,671,534 | G/C | — | uncertain significance |
| rs145467241 | 20:31,671,556 | G/T | — | likely benign |
| rs200543830 | 20:31,671,560 | G/A | — | uncertain significance |
| rs779744515 | 20:31,671,634 | G/A | — | uncertain significance |
| rs2516072169 | 20:31,671,650 | G/A | — | uncertain significance |
| rs200122108 | 20:31,671,677 | C/T | — | uncertain significance |
| rs567934675 | 20:31,672,298 | G/A | — | — |
| rs146428047 | 20:31,672,726 | C/T | — | uncertain significance |
| rs752406178 | 20:31,672,738 | C/T | — | uncertain significance |
| rs148384178 | 20:31,673,864 | A/G | — | uncertain significance |
| rs1375505290 | 20:31,673,879 | C/G | — | uncertain significance |
| rs202190359 | 20:31,673,909 | C/T | — | uncertain significance |
| rs543633125 | 20:31,676,783 | A/G | — | uncertain significance |
| rs181836133 | 20:31,676,818 | G/A | — | likely benign |
| rs146005184 | 20:31,679,987 | A/G | intron variant | — |
| rs1172805444 | 20:31,680,398 | C/G | — | uncertain significance |
| rs1258636861 | 20:31,685,450 | C/T | — | uncertain significance |
| rs374027770 | 20:31,685,544 | T/C | — | uncertain significance |
| rs142517837 | 20:31,685,586 | T/C | — | uncertain significance |
| rs370431635 | 20:31,688,259 | A/G | — | uncertain significance |
| rs2516091127 | 20:31,690,792 | T/A | — | uncertain significance |
| rs758458637 | 20:31,690,809 | G/A | — | uncertain significance |
| rs116725367 | 20:31,692,622 | C/T | — | uncertain significance |
| rs2424961 | 20:31,694,060 | C/T | regulatory region variant | — |
| rs767664604 | 20:31,695,613 | T/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.