APOL6
apolipoprotein L6
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 Variants42 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs763919417 | 22:36,052,486 | C/T | — | uncertain significance |
| rs778101319 | 22:36,052,506 | G/A | — | uncertain significance |
| rs764855542 | 22:36,054,693 | G/A | — | uncertain significance |
| rs373548173 | 22:36,054,708 | G/A | — | likely benign |
| rs1024852796 | 22:36,054,715 | T/C | — | uncertain significance |
| rs779047404 | 22:36,054,723 | G/A | — | likely benign |
| rs1269270139 | 22:36,054,827 | G/T | — | uncertain significance |
| rs2518090458 | 22:36,054,845 | C/G | — | uncertain significance |
| rs143660228 | 22:36,054,862 | C/T | — | likely benign |
| rs201547425 | 22:36,054,874 | C/G | — | uncertain significance |
| rs758605616 | 22:36,054,907 | C/T | — | uncertain significance |
| rs778035401 | 22:36,054,916 | C/A | — | uncertain significance |
| rs200805851 | 22:36,054,945 | G/A | — | likely benign |
| rs771515130 | 22:36,054,986 | C/T | — | likely benign |
| rs370134377 | 22:36,055,006 | G/A | — | likely benign |
| rs1189033247 | 22:36,055,027 | A/G | — | uncertain significance |
| rs751750988 | 22:36,055,032 | C/T | — | uncertain significance |
| rs186819188 | 22:36,055,036 | C/T | — | likely benign |
| rs191640929 | 22:36,055,077 | G/A | — | uncertain significance |
| rs761950647 | 22:36,055,107 | G/C | — | uncertain significance |
| rs184909665 | 22:36,055,141 | C/A | — | uncertain significance |
| rs780093200 | 22:36,055,153 | C/A | — | uncertain significance |
| rs192850920 | 22:36,055,168 | G/A | — | uncertain significance |
| rs200170835 | 22:36,055,197 | C/T | — | uncertain significance |
| rs762282595 | 22:36,055,206 | A/C | — | uncertain significance |
| rs773507616 | 22:36,055,219 | G/A | — | uncertain significance |
| rs748819725 | 22:36,055,227 | A/G | — | uncertain significance |
| rs145863080 | 22:36,055,257 | G/A | — | uncertain significance |
| rs558213377 | 22:36,055,267 | A/G | — | uncertain significance |
| rs200520869 | 22:36,055,294 | C/T | — | likely benign |
| rs996121781 | 22:36,055,298 | G/A | — | uncertain significance |
| rs143314363 | 22:36,055,320 | G/A | — | uncertain significance |
| rs2518091640 | 22:36,055,410 | T/G | — | uncertain significance |
| rs138269979 | 22:36,055,415 | G/A | — | likely benign |
| rs143747983 | 22:36,055,507 | G/T | — | uncertain significance |
| rs368285618 | 22:36,055,509 | G/T | — | uncertain significance |
| rs368095413 | 22:36,055,537 | G/A | — | uncertain significance |
| rs756351017 | 22:36,055,608 | T/G | — | uncertain significance |
| rs1470652307 | 22:36,055,627 | A/C | — | uncertain significance |
| rs5999924 | 22:36,056,144 | A/G | — | — |
| rs5750146 | 22:36,056,728 | G/A | 3 prime UTR variant | — |
| rs35807627 | 22:36,062,444 | C/T | 3 prime UTR variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.