SNX8
sorting nexin 8
Summary
Enables identical protein binding activity and phosphatidylinositol binding activity. Involved in early endosome to Golgi transport and intracellular protein transport. Located in early endosome membrane and retromer complex. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants45 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs894776378 | 7:2,294,708 | C/T | — | uncertain significance |
| rs144465573 | 7:2,294,712 | C/T | — | likely benign |
| rs2302070 | 7:2,296,493 | G/A | — | benign |
| rs115870022 | 7:2,296,500 | C/A | — | benign |
| rs767653352 | 7:2,296,531 | G/A | — | uncertain significance |
| rs764708647 | 7:2,296,534 | T/G | — | uncertain significance |
| rs144787122 | 7:2,296,552 | A/G | missense variant | — |
| rs769454131 | 7:2,296,588 | T/A | — | uncertain significance |
| rs766575430 | 7:2,296,615 | G/T | — | uncertain significance |
| rs777134047 | 7:2,297,037 | G/A | — | uncertain significance |
| rs1192804716 | 7:2,297,052 | G/A | — | likely benign |
| rs746184528 | 7:2,297,053 | C/A | — | uncertain significance |
| rs757963243 | 7:2,297,127 | T/C | — | uncertain significance |
| rs926988011 | 7:2,297,435 | T/G | — | uncertain significance |
| rs2398668 | 7:2,298,227 | C/T | regulatory region variant | — |
| rs77610730 | 7:2,299,301 | G/C | — | — |
| rs770286135 | 7:2,302,882 | C/T | — | uncertain significance |
| rs371599582 | 7:2,302,895 | G/T | — | uncertain significance |
| rs144726486 | 7:2,302,956 | G/C | — | uncertain significance |
| rs368408960 | 7:2,302,980 | G/C | — | uncertain significance |
| rs753488416 | 7:2,303,964 | C/T | — | uncertain significance |
| rs139054880 | 7:2,303,984 | G/A | — | uncertain significance |
| rs1795413290 | 7:2,304,008 | C/T | — | uncertain significance |
| rs753591171 | 7:2,304,068 | G/A | — | uncertain significance |
| rs35841174 | 7:2,304,077 | T/A | — | uncertain significance |
| rs774010540 | 7:2,309,200 | C/A | — | uncertain significance |
| rs752909431 | 7:2,309,264 | T/C | — | uncertain significance |
| rs2534294958 | 7:2,309,274 | C/T | — | uncertain significance |
| rs757423561 | 7:2,311,493 | T/C | — | uncertain significance |
| rs2534302336 | 7:2,311,529 | A/G | — | uncertain significance |
| rs776084789 | 7:2,311,543 | C/T | — | uncertain significance |
| rs2534302744 | 7:2,311,598 | C/G | — | uncertain significance |
| rs771225939 | 7:2,314,825 | C/T | — | uncertain significance |
| rs761714694 | 7:2,314,849 | C/G | — | uncertain significance |
| rs112173284 | 7:2,317,738 | G/A | — | benign |
| rs141606164 | 7:2,317,746 | C/G | — | uncertain significance |
| rs752761649 | 7:2,317,916 | T/C | — | uncertain significance |
| rs1174171980 | 7:2,317,928 | G/C | — | uncertain significance |
| rs117886084 | 7:2,317,934 | A/G | — | benign |
| rs1208805700 | 7:2,336,387 | T/A | — | — |
| rs62442539 | 7:2,352,594 | G/T | — | — |
| rs953207659 | 7:2,354,016 | A/C | — | uncertain significance |
| rs540088947 | 7:2,354,025 | G/C | — | uncertain significance |
| rs1014198822 | 7:2,354,039 | C/T | — | uncertain significance |
| rs55871547 | 7:2,354,352 | C/G | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.