NXPE4
neurexophilin and PC-esterase domain family member 4
Summary
Located in extracellular exosome. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants41 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs201894163 | 11:114,441,698 | C/T | — | likely benign |
| rs763146490 | 11:114,441,723 | A/C | — | uncertain significance |
| rs543250723 | 11:114,441,763 | A/G | — | uncertain significance |
| rs766558030 | 11:114,441,811 | T/A | — | uncertain significance |
| rs757098773 | 11:114,441,839 | T/C | — | uncertain significance |
| rs1948874944 | 11:114,441,892 | G/A | — | uncertain significance |
| rs1452906515 | 11:114,441,893 | T/G | — | uncertain significance |
| rs747828133 | 11:114,441,989 | C/G | — | uncertain significance |
| rs749708679 | 11:114,442,006 | A/G | — | uncertain significance |
| rs1948878550 | 11:114,442,021 | C/T | — | uncertain significance |
| rs1187422516 | 11:114,442,025 | C/T | — | uncertain significance |
| rs1474476951 | 11:114,442,039 | G/A | — | likely benign |
| rs2497078348 | 11:114,442,063 | T/G | — | uncertain significance |
| rs895192018 | 11:114,442,067 | C/G | — | uncertain significance |
| rs768723916 | 11:114,450,878 | C/T | — | uncertain significance |
| rs759279646 | 11:114,450,889 | C/T | — | uncertain significance |
| rs201579260 | 11:114,450,890 | G/A | — | uncertain significance |
| rs1250311890 | 11:114,450,898 | G/C | — | uncertain significance |
| rs2497136222 | 11:114,451,013 | T/C | — | uncertain significance |
| rs752723371 | 11:114,451,046 | T/C | — | likely benign |
| rs1356270641 | 11:114,453,088 | C/T | — | uncertain significance |
| rs368421021 | 11:114,453,206 | T/C | — | uncertain significance |
| rs776448352 | 11:114,453,290 | G/A | — | uncertain significance |
| rs565925125 | 11:114,453,360 | G/T | — | uncertain significance |
| rs200548586 | 11:114,453,403 | G/A | — | uncertain significance |
| rs778259672 | 11:114,453,406 | G/A | — | uncertain significance |
| rs111330181 | 11:114,453,455 | G/A | — | uncertain significance |
| rs201549180 | 11:114,453,511 | G/A | — | uncertain significance |
| rs972637851 | 11:114,453,551 | C/T | — | uncertain significance |
| rs191556206 | 11:114,453,556 | G/A | — | uncertain significance |
| rs1295011526 | 11:114,453,614 | T/C | — | uncertain significance |
| rs370550628 | 11:114,453,626 | T/C | — | uncertain significance |
| rs758803514 | 11:114,453,627 | T/A | — | uncertain significance |
| rs761351977 | 11:114,453,737 | A/G | — | uncertain significance |
| rs1412471587 | 11:114,453,738 | C/G | — | uncertain significance |
| rs762658104 | 11:114,465,388 | T/C | — | uncertain significance |
| rs774745312 | 11:114,465,394 | A/G | — | uncertain significance |
| rs2497239928 | 11:114,465,436 | A/G | — | uncertain significance |
| rs113520822 | 11:114,481,378 | C/T | regulatory region variant | — |
| rs141279402 | 11:114,530,596 | C/T | intergenic variant | — |
| rs185718408 | 11:114,534,749 | C/G | intergenic variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.