BPIFB2
BPI fold containing family B member 2
Summary
This gene encodes a member of the lipid transfer/lipopolysaccharide binding protein (LT/LBP) gene family. It is highly expressed in hypertrophic tonsils. This gene and three other members of the LT/LBP gene family form a cluster on the long arm of chromosome 20. [provided by RefSeq, Jul 2008]
Known Variants28 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs149889663 | 20:31,596,430 | T/A | — | likely benign |
| rs565493383 | 20:31,596,435 | G/A | — | likely benign |
| rs373825975 | 20:31,596,442 | C/T | — | uncertain significance |
| rs181110734 | 20:31,596,463 | G/A | — | uncertain significance |
| rs372044696 | 20:31,598,859 | C/T | — | uncertain significance |
| rs202092895 | 20:31,598,860 | G/A | — | uncertain significance |
| rs1051126120 | 20:31,598,862 | G/T | — | uncertain significance |
| rs368543110 | 20:31,598,897 | G/T | — | uncertain significance |
| rs375320227 | 20:31,600,637 | C/T | — | uncertain significance |
| rs142593623 | 20:31,601,644 | C/T | — | uncertain significance |
| rs763583629 | 20:31,601,668 | C/T | — | uncertain significance |
| rs1990321944 | 20:31,601,705 | G/A | — | uncertain significance |
| rs769557556 | 20:31,601,737 | G/A | — | uncertain significance |
| rs1201060049 | 20:31,603,296 | T/G | — | likely benign |
| rs576456659 | 20:31,604,551 | C/T | — | — |
| rs746264484 | 20:31,606,082 | C/A | — | uncertain significance |
| rs764051345 | 20:31,606,130 | A/G | — | uncertain significance |
| rs770303903 | 20:31,606,483 | C/T | — | uncertain significance |
| rs776452780 | 20:31,606,524 | G/A | — | likely benign |
| rs759107557 | 20:31,606,527 | G/C | — | uncertain significance |
| rs1028323471 | 20:31,606,552 | C/T | — | uncertain significance |
| rs367964762 | 20:31,606,585 | T/C | — | uncertain significance |
| rs371717562 | 20:31,606,593 | G/A | — | uncertain significance |
| rs141388517 | 20:31,607,410 | A/G | — | uncertain significance |
| rs148403687 | 20:31,608,388 | A/T | — | uncertain significance |
| rs747617309 | 20:31,609,529 | C/T | — | uncertain significance |
| rs974740970 | 20:31,609,559 | G/C | — | uncertain significance |
| rs553351251 | 20:31,609,568 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.