F9 c.521-362A>C

Variant ID: X-138632859-A-C

NM_000133.3(F9):c.521-362A>C

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Facets of individual-specific health signatures determined from longitudinal plasma proteome profiling.

Ebiomedicine
Dodig-Crnković, Tea T; Hong, Mun-Gwan MG; Thomas, Cecilia Engel CE; Häussler, Ragna S RS; Bendes, Annika A; Dale, Matilda M; Edfors, Fredrik F; Forsström, Björn B; Magnusson, Patrik K E PKE; Schuppe-Koistinen, Ina I; Odeberg, Jacob J; Fagerberg, Linn L; Gummesson, Anders A; Bergström, Göran G; Uhlén, Mathias M; Schwenk, Jochen M JM
Publication Date: 2020-07

Variant appearance in text: rs422187
PubMed Link: 32629387
Variant Present in the following documents:
  • Main text
  • main.pdf
View BVdb publication page



F9 Malmö, factor IX and deep vein thrombosis.

Haematologica
Bezemer, Irene D ID; Arellano, Andre R AR; Tong, Carmen H CH; Rowland, Charles M CM; Ireland, Helen A HA; Bauer, Kenneth A KA; Catanese, Joseph J; Reitsma, Pieter H PH; Doggen, Carine J M CJ; Devlin, James J JJ; Rosendaal, Frits R FR; Bare, Lance A LA
Publication Date: 2009-05

Variant appearance in text: rs422187
PubMed Link: 19286883
Variant Present in the following documents:
  • Main text
View BVdb publication page



Association of warfarin dose with genes involved in its action and metabolism.

Human Genetics
Wadelius, Mia M; Chen, Leslie Y LY; Eriksson, Niclas N; Bumpstead, Suzannah S; Ghori, Jilur J; Wadelius, Claes C; Bentley, David D; McGinnis, Ralph R; Deloukas, Panos P
Publication Date: 2007-03

Variant appearance in text: rs422187
PubMed Link: 17048007
Variant Present in the following documents:
View BVdb publication page