APOL5
apolipoprotein L5
Summary
This gene is a member of the apolipoprotein L gene family. The encoded protein is found in the cytoplasm, where it may affect the movement of lipids or allow the binding of lipids to organelles. [provided by RefSeq, Jul 2008]
Known Variants33 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs776279359 | 22:36,113,929 | G/C | — | uncertain significance |
| rs1176348620 | 22:36,113,956 | G/A | — | uncertain significance |
| rs768415716 | 22:36,116,648 | G/A | — | uncertain significance |
| rs139593449 | 22:36,116,662 | G/A | — | uncertain significance |
| rs763071253 | 22:36,116,681 | A/T | — | uncertain significance |
| rs781510344 | 22:36,122,308 | A/G | — | likely benign |
| rs148423435 | 22:36,122,330 | G/T | — | uncertain significance |
| rs769092389 | 22:36,122,346 | T/A | — | uncertain significance |
| rs5999985 | 22:36,122,356 | G/A | — | benign |
| rs369534518 | 22:36,122,366 | G/A | — | uncertain significance |
| rs2518143604 | 22:36,122,390 | A/G | — | uncertain significance |
| rs1230323364 | 22:36,122,420 | T/G | — | uncertain significance |
| rs887484530 | 22:36,122,509 | G/A | — | likely benign |
| rs761542526 | 22:36,122,515 | C/T | — | uncertain significance |
| rs141273692 | 22:36,122,548 | G/A | — | uncertain significance |
| rs2518144415 | 22:36,122,619 | G/A | — | uncertain significance |
| rs747447777 | 22:36,122,693 | G/A | — | uncertain significance |
| rs1393945495 | 22:36,122,708 | C/G | — | uncertain significance |
| rs369158723 | 22:36,122,726 | G/A | — | uncertain significance |
| rs142465276 | 22:36,122,761 | G/A | — | uncertain significance |
| rs144692919 | 22:36,122,791 | G/A | — | uncertain significance |
| rs1164803928 | 22:36,122,833 | A/C | — | uncertain significance |
| rs778849382 | 22:36,123,089 | C/T | — | uncertain significance |
| rs929513744 | 22:36,123,094 | G/C | — | uncertain significance |
| rs373982762 | 22:36,123,218 | G/T | — | uncertain significance |
| rs1927199883 | 22:36,123,223 | C/T | — | uncertain significance |
| rs1271778429 | 22:36,123,227 | T/G | — | uncertain significance |
| rs757370353 | 22:36,124,787 | C/T | — | uncertain significance |
| rs147690523 | 22:36,124,796 | G/A | — | uncertain significance |
| rs2518147437 | 22:36,124,844 | C/A | — | uncertain significance |
| rs370966999 | 22:36,124,847 | A/G | — | likely benign |
| rs200371039 | 22:36,124,878 | G/A | — | uncertain significance |
| rs2016586 | 22:36,125,264 | T/G | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.