APMAP
adipocyte plasma membrane associated protein
Summary
Enables arylesterase activity. Located in cell surface and membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants35 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs764444977 | 20:24,944,579 | C/T | — | uncertain significance |
| rs200397867 | 20:24,944,588 | C/T | — | uncertain significance |
| rs373605988 | 20:24,944,615 | C/T | — | uncertain significance |
| rs1385166674 | 20:24,944,618 | T/C | — | uncertain significance |
| rs775710141 | 20:24,944,621 | C/T | — | uncertain significance |
| rs553194798 | 20:24,944,622 | G/A | — | uncertain significance |
| rs372803829 | 20:24,949,666 | C/T | — | uncertain significance |
| rs6138438 | 20:24,949,944 | G/C | upstream gene variant | — |
| rs373986577 | 20:24,950,252 | A/G | — | uncertain significance |
| rs773138592 | 20:24,950,283 | C/G | — | uncertain significance |
| rs767448339 | 20:24,950,834 | G/A | — | uncertain significance |
| rs2514868620 | 20:24,950,851 | T/C | — | uncertain significance |
| rs779248044 | 20:24,950,875 | C/T | — | uncertain significance |
| rs149459666 | 20:24,950,900 | C/T | — | uncertain significance |
| rs200046619 | 20:24,952,135 | C/T | — | uncertain significance |
| rs2514869698 | 20:24,952,149 | G/A | — | uncertain significance |
| rs753353812 | 20:24,952,174 | C/T | — | uncertain significance |
| rs371061783 | 20:24,954,292 | G/A | — | uncertain significance |
| rs1464427832 | 20:24,954,325 | T/C | — | uncertain significance |
| rs185162626 | 20:24,954,344 | G/A | — | uncertain significance |
| rs751994228 | 20:24,954,364 | A/C | — | uncertain significance |
| rs56312312 | 20:24,959,386 | C/G | downstream gene variant | — |
| rs1179777073 | 20:24,959,416 | T/C | — | uncertain significance |
| rs139371606 | 20:24,959,426 | G/C | — | uncertain significance |
| rs547447032 | 20:24,963,805 | A/T | — | — |
| rs546068480 | 20:24,964,543 | G/T | — | uncertain significance |
| rs752583635 | 20:24,964,545 | G/C | — | uncertain significance |
| rs12242 | 20:24,964,558 | T/C | missense variant | — |
| rs774852463 | 20:24,964,578 | A/G | — | uncertain significance |
| rs758999671 | 20:24,964,603 | G/C | — | uncertain significance |
| rs777009862 | 20:24,964,609 | C/T | — | uncertain significance |
| rs750026402 | 20:24,973,275 | A/G | — | uncertain significance |
| rs990770069 | 20:24,973,290 | G/A | — | uncertain significance |
| rs2514887220 | 20:24,973,320 | C/T | — | uncertain significance |
| rs185515630 | 20:24,973,571 | T/C | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.