NXPE2
neurexophilin and PC-esterase domain family member 2
Summary
Predicted to be located in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants48 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs11215010 | 11:114,352,249 | T/C | intergenic variant | — |
| rs7948204 | 11:114,368,569 | T/C | intergenic variant | — |
| rs12420560 | 11:114,385,999 | G/A | upstream gene variant | — |
| rs12420571 | 11:114,386,029 | G/A | upstream gene variant | — |
| rs561722 | 11:114,386,830 | C/G | — | — |
| rs4466877 | 11:114,387,102 | G/A | upstream gene variant | — |
| rs12364094 | 11:114,435,644 | T/C | intergenic variant | — |
| rs10891700 | 11:114,437,886 | C/T | downstream gene variant | — |
| rs2135529674 | 11:114,550,452 | A/G | — | likely benign |
| rs556640570 | 11:114,568,798 | T/G | — | uncertain significance |
| rs758017057 | 11:114,568,891 | A/G | — | uncertain significance |
| rs772068009 | 11:114,568,894 | T/G | — | uncertain significance |
| rs2496838358 | 11:114,568,948 | C/T | — | uncertain significance |
| rs367916231 | 11:114,568,956 | A/G | — | uncertain significance |
| rs756651078 | 11:114,568,999 | C/T | — | uncertain significance |
| rs374127820 | 11:114,569,016 | C/A | — | uncertain significance |
| rs370835815 | 11:114,569,066 | A/T | — | uncertain significance |
| rs1340206242 | 11:114,569,098 | A/G | — | uncertain significance |
| rs750433667 | 11:114,569,221 | C/G | — | uncertain significance |
| rs1565388288 | 11:114,569,305 | G/A | — | uncertain significance |
| rs2496841109 | 11:114,569,308 | C/A | — | uncertain significance |
| rs774230603 | 11:114,569,401 | T/G | — | uncertain significance |
| rs756331151 | 11:114,569,416 | T/C | — | uncertain significance |
| rs1417592131 | 11:114,569,433 | A/T | — | uncertain significance |
| rs927561088 | 11:114,569,436 | C/T | — | uncertain significance |
| rs1403362060 | 11:114,574,751 | C/G | — | uncertain significance |
| rs1951424120 | 11:114,574,753 | A/C | — | uncertain significance |
| rs1449078847 | 11:114,574,765 | C/A | — | uncertain significance |
| rs374175174 | 11:114,576,530 | A/G | — | uncertain significance |
| rs2496872596 | 11:114,576,542 | A/G | — | uncertain significance |
| rs559523338 | 11:114,576,682 | C/A | — | uncertain significance |
| rs746249458 | 11:114,576,686 | A/G | — | uncertain significance |
| rs2496875551 | 11:114,577,150 | T/A | — | uncertain significance |
| rs952481685 | 11:114,577,163 | T/G | — | uncertain significance |
| rs773922645 | 11:114,577,270 | G/A | — | uncertain significance |
| rs1314343980 | 11:114,577,276 | T/C | — | uncertain significance |
| rs747484480 | 11:114,577,367 | G/C | — | uncertain significance |
| rs144998340 | 11:114,577,395 | C/T | — | likely benign |
| rs367906083 | 11:114,577,408 | G/A | — | uncertain significance |
| rs557302723 | 11:114,577,432 | T/A | — | uncertain significance |
| rs7108474 | 11:114,577,456 | T/C | — | likely benign |
| rs760559531 | 11:114,577,505 | T/A | — | uncertain significance |
| rs376335149 | 11:114,577,517 | A/T | — | uncertain significance |
| rs201985306 | 11:114,577,601 | G/A | — | likely benign |
| rs1042879040 | 11:114,577,603 | A/T | — | uncertain significance |
| rs1352014307 | 11:114,577,645 | T/C | — | uncertain significance |
| rs1712790 | 11:114,621,469 | T/C | intergenic variant | — |
| rs187038512 | 11:114,679,675 | C/T | intergenic variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.