VWA7
von Willebrand factor A domain containing 7
Summary
Predicted to be located in extracellular region. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants60 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs3101017 | 6:31,733,466 | T/C | missense variant | — |
| rs2537510758 | 6:31,733,474 | G/A | — | uncertain significance |
| rs1194012366 | 6:31,733,520 | A/G | — | uncertain significance |
| rs28399998 | 6:31,733,689 | G/A | — | uncertain significance |
| rs140640408 | 6:31,733,713 | C/T | — | uncertain significance |
| rs145784901 | 6:31,733,722 | C/T | — | uncertain significance |
| rs531201783 | 6:31,733,758 | C/T | — | uncertain significance |
| rs1387144226 | 6:31,734,133 | G/A | — | uncertain significance |
| rs1178351176 | 6:31,734,242 | C/T | — | uncertain significance |
| rs758285570 | 6:31,734,301 | G/A | — | uncertain significance |
| rs3115671 | 6:31,734,345 | G/T | synonymous variant | — |
| rs767669981 | 6:31,734,367 | G/A | — | uncertain significance |
| rs547891848 | 6:31,734,391 | G/A | — | uncertain significance |
| rs369262187 | 6:31,734,401 | C/T | — | uncertain significance |
| rs779682085 | 6:31,734,412 | G/C | — | uncertain significance |
| rs769198360 | 6:31,734,413 | G/C | — | uncertain significance |
| rs993362892 | 6:31,734,509 | C/T | — | uncertain significance |
| rs751556994 | 6:31,734,941 | C/A | — | uncertain significance |
| rs746852554 | 6:31,735,153 | C/A | — | uncertain significance |
| rs1204004899 | 6:31,735,154 | C/A | — | uncertain significance |
| rs577797776 | 6:31,735,244 | G/A | — | uncertain significance |
| rs367830607 | 6:31,735,461 | A/T | — | uncertain significance |
| rs2151391508 | 6:31,735,507 | C/T | — | uncertain significance |
| rs1398112697 | 6:31,736,799 | G/A | — | uncertain significance |
| rs1811919978 | 6:31,736,877 | G/T | — | uncertain significance |
| rs1282878941 | 6:31,736,890 | C/T | — | uncertain significance |
| rs777539303 | 6:31,736,913 | G/A | — | uncertain significance |
| rs760103923 | 6:31,736,937 | C/T | — | uncertain significance |
| rs149469601 | 6:31,736,949 | C/T | — | uncertain significance |
| rs142871734 | 6:31,737,815 | C/T | — | uncertain significance |
| rs139629177 | 6:31,737,819 | C/A | — | uncertain significance |
| rs571937790 | 6:31,737,820 | C/G | — | uncertain significance |
| rs753382366 | 6:31,737,860 | G/A | — | uncertain significance |
| rs3130490 | 6:31,739,120 | G/T | intron variant | — |
| rs527960948 | 6:31,739,730 | G/C | — | — |
| rs538294600 | 6:31,739,794 | G/A | — | — |
| rs805825 | 6:31,740,454 | G/C | — | — |
| rs373169264 | 6:31,740,745 | G/A | — | uncertain significance |
| rs374709454 | 6:31,740,824 | C/T | — | uncertain significance |
| rs542536426 | 6:31,740,900 | C/T | — | likely benign |
| rs748856442 | 6:31,741,043 | C/T | — | uncertain significance |
| rs375719361 | 6:31,741,139 | G/A | — | uncertain significance |
| rs552048751 | 6:31,741,188 | C/A | — | uncertain significance |
| rs201605097 | 6:31,741,194 | G/C | — | uncertain significance |
| rs9469051 | 6:31,741,490 | G/A | — | — |
| rs707930 | 6:31,741,659 | C/A | — | — |
| rs6914412 | 6:31,742,242 | T/C | downstream gene variant | — |
| rs1812505505 | 6:31,742,298 | G/T | — | uncertain significance |
| rs777401252 | 6:31,742,328 | G/T | — | uncertain significance |
| rs201752222 | 6:31,742,354 | A/T | — | uncertain significance |
| rs707928 | 6:31,742,590 | A/G | downstream gene variant | — |
| rs9469052 | 6:31,743,844 | C/A | — | uncertain significance |
| rs974987576 | 6:31,743,879 | G/T | — | uncertain significance |
| rs141452479 | 6:31,743,895 | G/A | — | uncertain significance |
| rs1415619693 | 6:31,743,910 | T/C | — | uncertain significance |
| rs765685579 | 6:31,743,928 | C/T | — | uncertain significance |
| rs753200174 | 6:31,743,929 | G/A | — | uncertain significance |
| rs769559944 | 6:31,744,333 | T/A | — | uncertain significance |
| rs2537567564 | 6:31,744,363 | G/A | — | uncertain significance |
| rs1297128844 | 6:31,744,438 | G/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.