APOL2
apolipoprotein L2
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. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]
Known Variants35 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs200674632 | 22:36,623,476 | T/G | — | uncertain significance |
| rs367654498 | 22:36,623,622 | C/A | — | uncertain significance |
| rs200071618 | 22:36,623,628 | G/A | — | uncertain significance |
| rs772205206 | 22:36,623,629 | T/G | — | uncertain significance |
| rs201957684 | 22:36,623,704 | C/T | — | uncertain significance |
| rs1286886718 | 22:36,623,752 | C/T | — | uncertain significance |
| rs768405086 | 22:36,623,791 | G/A | — | uncertain significance |
| rs1033495952 | 22:36,623,814 | G/A | — | uncertain significance |
| rs374610829 | 22:36,623,841 | G/A | — | uncertain significance |
| rs368403887 | 22:36,623,842 | T/G | — | uncertain significance |
| rs570763468 | 22:36,623,857 | T/A | — | uncertain significance |
| rs973778659 | 22:36,623,926 | G/C | — | likely benign |
| rs764422788 | 22:36,623,928 | G/A | — | uncertain significance |
| rs555460579 | 22:36,623,947 | T/C | — | uncertain significance |
| rs746490357 | 22:36,623,974 | T/A | — | uncertain significance |
| rs2517864645 | 22:36,623,997 | C/T | — | uncertain significance |
| rs373647571 | 22:36,624,009 | C/A | — | uncertain significance |
| rs201782732 | 22:36,624,073 | T/A | — | likely benign |
| rs201222628 | 22:36,624,123 | G/A | — | uncertain significance |
| rs141853160 | 22:36,624,166 | G/A | — | uncertain significance |
| rs779279140 | 22:36,624,183 | T/C | — | uncertain significance |
| rs377630085 | 22:36,624,195 | C/G | — | uncertain significance |
| rs762361767 | 22:36,624,205 | G/A | — | uncertain significance |
| rs2517865390 | 22:36,624,208 | G/A | — | uncertain significance |
| rs118097350 | 22:36,624,231 | C/T | — | benign |
| rs201164781 | 22:36,624,242 | G/C | — | uncertain significance |
| rs778468395 | 22:36,624,258 | T/A | — | uncertain significance |
| rs749979854 | 22:36,624,306 | C/T | — | uncertain significance |
| rs199839971 | 22:36,624,307 | G/A | — | uncertain significance |
| rs756502784 | 22:36,627,387 | T/C | — | uncertain significance |
| rs768066276 | 22:36,627,456 | C/T | — | uncertain significance |
| rs756444914 | 22:36,627,464 | A/C | — | uncertain significance |
| rs2003813 | 22:36,628,993 | C/T | regulatory region variant | — |
| rs2157249 | 22:36,631,039 | T/C | intron variant | — |
| rs916264 | 22:36,633,836 | A/C | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.