PLCG2 c.3481+2513C>G

Variant ID: 16-81976177-C-G

NM_002661.3(PLCG2):c.3481+2513C>G

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Clinical and Genetic Risk Factors for Acute Incident Venous Thromboembolism in Ambulatory Patients With COVID-19.

Jama Internal Medicine
Xie, JunQing J; Prats-Uribe, Albert A; Feng, Qi Q; Wang, YunHe Y; Gill, Dipender D; Paredes, Roger R; Prieto-Alhambra, Dani D
Publication Date: 2022-10-01

Variant appearance in text: rs16956040
PubMed Link: 35980616
Variant Present in the following documents:
  • jamainternmed-e223858-s001.pdf
View BVdb publication page