VWF c.2186+2664G>A

Variant ID: 12-6159045-C-T

NM_000552.3(VWF):c.2186+2664G>A

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Genome-wide association studies identify genetic loci for low von Willebrand factor levels.

European Journal Of Human Genetics : Ejhg
van Loon, Janine J; Dehghan, Abbas A; Weihong, Tang T; Trompet, Stella S; McArdle, Wendy L WL; Asselbergs, Folkert W FW; Chen, Ming-Huei MH; Lopez, Lorna M LM; Huffman, Jennifer E JE; Leebeek, Frank W G FW; Basu, Saonli S; Stott, David J DJ; Rumley, Ann A; Gansevoort, Ron T RT; Davies, Gail G; Wilson, James J F JJ; Witteman, Jacqueline C M JC; Cao, Xiting X; de Craen, Anton J M AJ; Bakker, Stephan J L SJ; Psaty, Bruce M BM; Starr, John M JM; Hofman, Albert A; Wouter Jukema, J J; Deary, Ian J IJ; Hayward, Caroline C; van der Harst, Pim P; Lowe, Gordon D O GD; Folsom, Aaron R AR; Strachan, David P DP; Smith, Nicolas N; de Maat, Moniek P M MP; O'Donnell, Christopher C
Publication Date: 2016-07

Variant appearance in text: rs216303
PubMed Link: 26486471
Variant Present in the following documents:
  • Main text
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