PNLIPRP3
pancreatic lipase related protein 3
Summary
Predicted to enable lipoprotein lipase activity and phospholipase A1 activity. Predicted to be involved in several processes, including cholesterol homeostasis; high-density lipoprotein particle remodeling; and triglyceride catabolic process. Predicted to be located in extracellular region. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants32 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs775556545 | 10:118,187,538 | G/C | — | uncertain significance |
| rs753812607 | 10:118,196,249 | G/A | — | uncertain significance |
| rs749553166 | 10:118,196,334 | C/T | — | uncertain significance |
| rs374778789 | 10:118,196,337 | G/A | — | uncertain significance |
| rs776713019 | 10:118,196,355 | T/C | — | uncertain significance |
| rs61744026 | 10:118,199,261 | G/C | coding sequence variant | — |
| rs561218694 | 10:118,199,694 | T/C | — | — |
| rs373852386 | 10:118,202,577 | C/T | — | uncertain significance |
| rs2494125035 | 10:118,202,607 | A/G | — | uncertain significance |
| rs954954313 | 10:118,202,630 | C/T | — | uncertain significance |
| rs570400848 | 10:118,202,631 | G/A | — | uncertain significance |
| rs1438796930 | 10:118,203,924 | A/T | — | uncertain significance |
| rs185969436 | 10:118,203,934 | A/G | — | uncertain significance |
| rs200054779 | 10:118,203,969 | G/C | — | uncertain significance |
| rs551987600 | 10:118,211,134 | C/T | — | — |
| rs144686516 | 10:118,215,294 | C/A | — | uncertain significance |
| rs1387478139 | 10:118,215,319 | T/C | — | likely benign |
| rs544377195 | 10:118,220,495 | C/A | — | uncertain significance |
| rs149530976 | 10:118,220,689 | C/T | — | uncertain significance |
| rs1347041779 | 10:118,220,726 | T/A | — | uncertain significance |
| rs1589986756 | 10:118,220,738 | C/A | — | uncertain significance |
| rs117321115 | 10:118,224,507 | G/A | intron variant | — |
| rs748857257 | 10:118,225,652 | C/T | — | uncertain significance |
| rs2494177665 | 10:118,228,718 | A/G | — | uncertain significance |
| rs746584730 | 10:118,228,803 | A/G | — | uncertain significance |
| rs61864846 | 10:118,229,168 | C/T | intron variant | — |
| rs150059984 | 10:118,231,318 | G/A | — | likely benign |
| rs1437689947 | 10:118,236,171 | C/T | — | uncertain significance |
| rs377599210 | 10:118,236,204 | G/A | — | uncertain significance |
| rs758936524 | 10:118,236,226 | A/G | — | uncertain significance |
| rs1175174579 | 10:118,236,279 | A/G | — | uncertain significance |
| rs753083268 | 10:118,236,325 | G/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.