VWF c.4456_4458delinsAAC ;(p.S1486N)

Variant ID: 12-6128126-CGA-GTT

NM_000552.3(VWF):c.4456_4458delinsAAC;(p.S1486N)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Common and rare von Willebrand factor (VWF) coding variants, VWF levels, and factor VIII levels in African Americans: the NHLBI Exome Sequencing Project.

Blood
Johnsen, Jill M JM; Auer, Paul L PL; Morrison, Alanna C AC; Jiao, Shuo S; Wei, Peng P; Haessler, Jeffrey J; Fox, Keolu K; McGee, Sean R SR; Smith, Joshua D JD; Carlson, Christopher S CS; Smith, Nicholas N; Boerwinkle, Eric E; Kooperberg, Charles C; Nickerson, Deborah A DA; Rich, Stephen S SS; Green, David D; Peters, Ulrike U; Cushman, Mary M; Reiner, Alex P AP; ,
Publication Date: 2013-07-25

Variant appearance in text: VWF: Ser1486Asn
PubMed Link: 23690449
Variant Present in the following documents:
  • Main text
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