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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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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