NYAP2
neuronal tyrosine-phosphorylated phosphoinositide-3-kinase adaptor 2
Summary
Predicted to be involved in neuron projection morphogenesis and phosphatidylinositol 3-kinase/protein kinase B signal transduction. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants46 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs201512658 | 2:226,273,657 | C/G | — | uncertain significance |
| rs778592921 | 2:226,273,702 | A/G | — | uncertain significance |
| rs2470135763 | 2:226,273,774 | G/A | — | uncertain significance |
| rs375169851 | 2:226,273,790 | G/T | — | uncertain significance |
| rs13015496 | 2:226,290,705 | C/G | intron variant | — |
| rs6436554 | 2:226,297,013 | G/A | intron variant | — |
| rs12614411 | 2:226,297,530 | G/C | — | — |
| rs7420395 | 2:226,314,492 | C/T | intron variant | — |
| rs908639 | 2:226,315,266 | T/G | — | — |
| rs6729386 | 2:226,317,760 | G/A | regulatory region variant | — |
| rs6436561 | 2:226,370,779 | A/C | — | — |
| rs771022509 | 2:226,378,107 | G/A | — | uncertain significance |
| rs2469237579 | 2:226,378,215 | G/A | — | uncertain significance |
| rs766171317 | 2:226,378,260 | G/T | — | uncertain significance |
| rs2469346394 | 2:226,446,826 | G/A | — | uncertain significance |
| rs772989177 | 2:226,446,845 | C/A | — | uncertain significance |
| rs760467083 | 2:226,446,980 | G/T | — | likely benign |
| rs567364084 | 2:226,447,076 | C/T | — | uncertain significance |
| rs1395419658 | 2:226,447,233 | A/G | — | uncertain significance |
| rs1692308804 | 2:226,447,259 | G/C | — | uncertain significance |
| rs376429827 | 2:226,447,292 | G/A | — | uncertain significance |
| rs746284766 | 2:226,447,327 | C/G | — | likely benign |
| rs1692311648 | 2:226,447,338 | G/C | — | uncertain significance |
| rs367790714 | 2:226,447,359 | C/G | — | uncertain significance |
| rs377307715 | 2:226,447,398 | G/A | — | uncertain significance |
| rs750626822 | 2:226,447,446 | C/T | — | uncertain significance |
| rs759695162 | 2:226,447,575 | C/T | — | uncertain significance |
| rs371936878 | 2:226,447,628 | C/G | — | uncertain significance |
| rs773627897 | 2:226,447,638 | C/T | — | uncertain significance |
| rs138500026 | 2:226,447,641 | G/A | — | uncertain significance |
| rs2469349330 | 2:226,447,679 | A/C | — | uncertain significance |
| rs1420144648 | 2:226,447,680 | G/A | — | uncertain significance |
| rs563650514 | 2:226,447,682 | C/T | — | uncertain significance |
| rs12477972 | 2:226,482,872 | G/A | intron variant | — |
| rs2054079 | 2:226,486,752 | C/G | — | — |
| rs781079866 | 2:226,491,701 | A/G | — | uncertain significance |
| rs2469422640 | 2:226,491,711 | A/T | — | uncertain significance |
| rs1173602930 | 2:226,491,768 | G/A | — | uncertain significance |
| rs372836261 | 2:226,491,825 | C/T | — | uncertain significance |
| rs200066611 | 2:226,516,181 | C/T | — | uncertain significance |
| rs61753536 | 2:226,516,188 | G/C | — | benign |
| rs1216355535 | 2:226,516,198 | C/T | — | uncertain significance |
| rs2469462341 | 2:226,516,235 | A/T | — | uncertain significance |
| rs2469462370 | 2:226,516,249 | C/G | — | uncertain significance |
| rs200139665 | 2:226,516,274 | G/A | — | uncertain significance |
| rs2014896 | 2:226,530,275 | C/T | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.