RASIP1 c.823+1211G>C

Variant ID: 19-49241006-C-G

NM_017805.2(RASIP1):c.823+1211G>C

This variant was identified in 2 publications

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: rs12981072
PubMed Link: 35980616
Variant Present in the following documents:
  • jamainternmed-e223858-s001.pdf
View BVdb publication page



Somatic Mutation Profiling of Papillary Thyroid Carcinomas by Whole-exome Sequencing and Its Relationship with Clinical Characteristics.

International Journal Of Medical Sciences
Qi, Tingyue T; Rong, Xin X; Feng, Qingling Q; Sun, Hongguang H; Cao, Haiyan H; Yang, Yan Y; Feng, Hao H; Zhu, Linhai L; Wang, Lei L; Du, Qiu Q
Publication Date: 2021

Variant appearance in text: rs12981072
PubMed Link: 34104084
Variant Present in the following documents:
  • ijmsv18p2532s2.xlsx, sheet 1
View BVdb publication page