BPI
bactericidal permeability increasing protein
Summary
This gene encodes a lipopolysaccharide binding protein. It is associated with human neutrophil granules and has antimicrobial activity against gram-negative organisms. [provided by RefSeq, Nov 2014]
Known Variants54 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs199723457 | 20:36,932,620 | G/A | — | uncertain significance |
| rs1430795530 | 20:36,932,630 | C/A | — | uncertain significance |
| rs5743497 | 20:36,932,647 | G/A | — | benign |
| rs5743498 | 20:36,932,648 | C/T | — | benign |
| rs1341023 | 20:36,932,660 | C/T | missense variant | benign |
| rs1341024 | 20:36,932,676 | G/C | — | benign |
| rs758217676 | 20:36,932,677 | G/A | — | uncertain significance |
| rs1422612044 | 20:36,932,686 | G/A | — | uncertain significance |
| rs549000920 | 20:36,932,692 | G/A | — | likely benign |
| rs771157781 | 20:36,932,702 | C/T | — | uncertain significance |
| rs1169744542 | 20:36,932,738 | A/G | — | uncertain significance |
| rs5743500 | 20:36,937,342 | C/T | — | benign |
| rs761505075 | 20:36,937,385 | A/G | — | uncertain significance |
| rs148087853 | 20:36,937,413 | C/G | — | uncertain significance |
| rs5743502 | 20:36,937,431 | C/T | — | benign |
| rs760852444 | 20:36,938,903 | G/A | — | uncertain significance |
| rs764359200 | 20:36,938,913 | A/C | — | uncertain significance |
| rs5743506 | 20:36,938,924 | G/C | — | benign |
| rs193123151 | 20:36,938,928 | G/C | — | uncertain significance |
| rs2515875439 | 20:36,938,968 | C/T | — | likely benign |
| rs142530722 | 20:36,938,971 | G/A | — | likely benign |
| rs5743507 | 20:36,939,052 | G/C | — | benign |
| rs1477203371 | 20:36,940,284 | T/C | — | uncertain significance |
| rs5743509 | 20:36,940,314 | C/T | — | benign |
| rs116381416 | 20:36,944,749 | C/A | intron variant | — |
| rs772370916 | 20:36,946,821 | G/A | — | likely benign |
| rs372552649 | 20:36,946,837 | C/T | — | uncertain significance |
| rs4358188 | 20:36,946,848 | G/A | missense variant | benign |
| rs111327200 | 20:36,946,875 | C/A | — | uncertain significance |
| rs150340828 | 20:36,946,885 | G/T | — | benign |
| rs746839185 | 20:36,948,608 | G/C | — | uncertain significance |
| rs2076674401 | 20:36,948,642 | C/T | — | uncertain significance |
| rs5743511 | 20:36,948,934 | G/C | intron variant | — |
| rs1457689372 | 20:36,952,327 | T/C | — | uncertain significance |
| rs142882330 | 20:36,952,338 | G/A | — | likely benign |
| rs2076699459 | 20:36,952,349 | C/G | — | uncertain significance |
| rs765711506 | 20:36,952,355 | G/T | — | uncertain significance |
| rs1333560086 | 20:36,952,413 | G/T | — | uncertain significance |
| rs2515898318 | 20:36,952,438 | G/C | — | likely benign |
| rs5743514 | 20:36,952,454 | G/A | — | uncertain significance |
| rs1385863698 | 20:36,953,204 | C/A | — | uncertain significance |
| rs5743521 | 20:36,953,495 | A/T | intron variant | — |
| rs62201523 | 20:36,953,681 | C/T | — | — |
| rs137967923 | 20:36,954,670 | G/A | — | likely benign |
| rs775959420 | 20:36,954,674 | A/G | — | uncertain significance |
| rs755860983 | 20:36,954,747 | C/T | — | likely benign |
| rs150094771 | 20:36,954,748 | G/A | — | uncertain significance |
| rs747746264 | 20:36,954,820 | T/G | — | uncertain significance |
| rs6024905 | 20:36,957,837 | G/A | upstream gene variant | — |
| rs771114514 | 20:36,959,489 | C/G | — | uncertain significance |
| rs538018088 | 20:36,961,720 | C/T | — | — |
| rs5743542 | 20:36,964,002 | A/G | — | conflicting classifications of pathogenicity |
| rs200632000 | 20:36,964,056 | G/A | — | uncertain significance |
| rs199545210 | 20:36,965,551 | T/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.