XKR6
XK related 6
Summary
Predicted to be involved in apoptotic process involved in development; engulfment of apoptotic cell; and phosphatidylserine exposure on apoptotic cell surface. Predicted to be located in membrane. Predicted to be active in plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants74 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs7014968 | 8:10,754,511 | C/G | — | — |
| rs757566491 | 8:10,755,493 | T/C | — | uncertain significance |
| rs578022670 | 8:10,755,530 | C/T | — | uncertain significance |
| rs1217951730 | 8:10,755,601 | G/C | — | uncertain significance |
| rs1799938300 | 8:10,755,649 | G/A | — | uncertain significance |
| rs199912681 | 8:10,755,653 | G/A | — | uncertain significance |
| rs905865631 | 8:10,755,674 | T/A | — | uncertain significance |
| rs200086321 | 8:10,755,724 | G/A | — | uncertain significance |
| rs775000168 | 8:10,755,760 | G/A | — | uncertain significance |
| rs1220861460 | 8:10,755,845 | C/T | — | uncertain significance |
| rs748299780 | 8:10,755,923 | C/T | — | uncertain significance |
| rs138547627 | 8:10,755,931 | G/A | — | uncertain significance |
| rs767517055 | 8:10,755,991 | G/A | — | uncertain significance |
| rs760579845 | 8:10,756,018 | G/A | — | uncertain significance |
| rs780603148 | 8:10,756,066 | C/T | — | uncertain significance |
| rs377201022 | 8:10,756,180 | T/C | — | uncertain significance |
| rs377188885 | 8:10,756,220 | C/T | — | uncertain significance |
| rs2536123921 | 8:10,756,223 | A/G | — | uncertain significance |
| rs2536124234 | 8:10,756,330 | C/T | — | uncertain significance |
| rs767011160 | 8:10,756,346 | C/T | — | uncertain significance |
| rs1799958467 | 8:10,756,360 | C/T | — | uncertain significance |
| rs779390900 | 8:10,756,361 | G/A | — | uncertain significance |
| rs6997839 | 8:10,766,028 | T/A | — | — |
| rs4240671 | 8:10,767,748 | G/A | regulatory region variant | — |
| rs7821826 | 8:10,769,439 | C/T | intron variant | — |
| rs6992403 | 8:10,790,758 | C/G | — | — |
| rs6980908 | 8:10,795,475 | C/T | — | — |
| rs7000772 | 8:10,795,613 | A/G | — | — |
| rs73196840 | 8:10,801,658 | A/C | intron variant | — |
| rs56084964 | 8:10,810,066 | C/G | intron variant | — |
| rs60724652 | 8:10,810,249 | A/T | intron variant | — |
| rs35910832 | 8:10,813,197 | T/G | — | — |
| rs6982751 | 8:10,813,474 | C/G | intron variant | — |
| rs10107658 | 8:10,815,146 | G/T | — | — |
| rs4434585 | 8:10,816,050 | A/C | — | — |
| rs4314618 | 8:10,816,772 | A/G | intron variant | — |
| rs4078189 | 8:10,833,489 | A/C | intron variant | — |
| rs4451267 | 8:10,835,917 | C/T | intron variant | — |
| rs4841468 | 8:10,846,709 | C/A | intron variant | — |
| rs56278516 | 8:10,846,958 | T/A | — | — |
| rs3923921 | 8:10,849,486 | T/C | intron variant | — |
| rs61427182 | 8:10,866,603 | G/C | — | — |
| rs12216784 | 8:10,868,737 | G/C | intron variant | — |
| rs11784312 | 8:10,872,767 | G/A | regulatory region variant | — |
| rs4076425 | 8:10,879,857 | G/A | intron variant | — |
| rs73196896 | 8:10,894,453 | C/G | upstream gene variant | — |
| rs4841485 | 8:10,909,936 | T/C | intron variant | — |
| rs7462931 | 8:10,910,343 | G/A | — | — |
| rs577065877 | 8:10,910,638 | C/T | — | — |
| rs4262293 | 8:10,935,687 | T/A | — | — |
| rs4840543 | 8:10,954,994 | A/T | intron variant | — |
| rs10087081 | 8:10,974,917 | C/T | intron variant | — |
| rs60383089 | 8:10,983,579 | T/C | — | — |
| rs7460469 | 8:11,027,441 | G/A | intron variant | — |
| rs10108347 | 8:11,033,517 | G/C | downstream gene variant | — |
| rs2409722 | 8:11,039,816 | T/G | intron variant | — |
| rs7819412 | 8:11,045,161 | G/A | intron variant | — |
| rs768684995 | 8:11,058,175 | G/A | — | uncertain significance |
| rs369205575 | 8:11,058,203 | C/T | — | uncertain significance |
| rs2486466136 | 8:11,058,263 | C/A | — | uncertain significance |
| rs1169962022 | 8:11,058,425 | C/G | — | uncertain significance |
| rs775232665 | 8:11,058,503 | C/G | — | likely benign |
| rs2486468239 | 8:11,058,514 | G/T | — | uncertain significance |
| rs2117176244 | 8:11,058,524 | T/G | — | uncertain significance |
| rs758611449 | 8:11,058,533 | G/T | — | uncertain significance |
| rs1302980506 | 8:11,058,581 | C/T | — | uncertain significance |
| rs970451976 | 8:11,058,602 | G/T | — | uncertain significance |
| rs2486469385 | 8:11,058,610 | C/T | — | likely benign |
| rs1458290784 | 8:11,058,620 | G/A | — | uncertain significance |
| rs1308302694 | 8:11,058,629 | G/C | — | uncertain significance |
| rs893277866 | 8:11,058,734 | A/C | — | uncertain significance |
| rs1169355858 | 8:11,058,746 | C/G | — | uncertain significance |
| rs1452476398 | 8:11,058,760 | T/C | — | uncertain significance |
| rs753589511 | 8:11,058,764 | C/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.