PSMD13 c.175-773T>G

Variant ID: 11-243268-T-G

NM_002817.3(PSMD13):c.175-773T>G

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Rare and low-frequency coding variants in CXCR2 and other genes are associated with hematological traits.

Nature Genetics
Auer, Paul L PL; Teumer, Alexander A; Schick, Ursula U; O'Shaughnessy, Andrew A; Lo, Ken Sin KS; Chami, Nathalie N; Carlson, Chris C; de Denus, Simon S; Dubé, Marie-Pierre MP; Haessler, Jeff J; Jackson, Rebecca D RD; Kooperberg, Charles C; Perreault, Louis-Philippe Lemieux LP; Nauck, Matthias M; Peters, Ulrike U; Rioux, John D JD; Schmidt, Frank F; Turcot, Valérie V; Völker, Uwe U; Völzke, Henry H; Greinacher, Andreas A; Hsu, Li L; Tardif, Jean-Claude JC; Diaz, George A GA; Reiner, Alexander P AP; Lettre, Guillaume G
Publication Date: 2014-06

Variant appearance in text: rs505404
PubMed Link: 24777453
Variant Present in the following documents:
  • NIHMS581495-supplement-1.pdf
View BVdb publication page



A genome- and phenome-wide association study to identify genetic variants influencing platelet count and volume and their pleiotropic effects.

Human Genetics
Shameer, Khader K; Denny, Joshua C JC; Ding, Keyue K; Jouni, Hayan H; Crosslin, David R DR; de Andrade, Mariza M; Chute, Christopher G CG; Peissig, Peggy P; Pacheco, Jennifer A JA; Li, Rongling R; Bastarache, Lisa L; Kho, Abel N AN; Ritchie, Marylyn D MD; Masys, Daniel R DR; Chisholm, Rex L RL; Larson, Eric B EB; McCarty, Catherine A CA; Roden, Dan M DM; Jarvik, Gail P GP; Kullo, Iftikhar J IJ
Publication Date: 2014-01

Variant appearance in text: rs505404
PubMed Link: 24026423
Variant Present in the following documents:
  • Main text
View BVdb publication page