PCSK7 c.1534+3912T>G

Variant ID: 11-117085270-A-C

NM_004716.2(PCSK7):c.1534+3912T>G

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Acute Coronary Syndrome: Unravelling the Biology to Identify New Therapies.

Cells
Tucker, Bradley B; Patel, Sanjay S
Publication Date: 2022-12-19

Variant appearance in text: rs236911
PubMed Link: 36552899
Variant Present in the following documents:
  • Main text
  • cells-11-04136.pdf
View BVdb publication page



The rs508487, rs236911, and rs236918 Genetic Variants of the Proprotein Convertase Subtilisin-Kexin Type 7 (PCSK7) Gene Are Associated with Acute Coronary Syndrome and with Plasma Concentrations of HDL-Cholesterol and Triglycerides.

Cells
Vargas-Alarcón, Gilberto G; Pérez-Méndez, Oscar O; González-Pacheco, Héctor H; Ramírez-Bello, Julián J; Posadas-Sánchez, Rosalinda R; Escobedo, Galileo G; Fragoso, José Manuel JM
Publication Date: 2021-06-09

Variant appearance in text: rs236911
PubMed Link: 34207761
Variant Present in the following documents:
  • Main text
  • cells-10-01444.pdf
View BVdb publication page



Mouse Models of Human Proprotein Convertase Insufficiency.

Endocrine Reviews
Shakya, Manita M; Lindberg, Iris I
Publication Date: 2021-05-25

Variant appearance in text: rs236911
PubMed Link: 33382413
Variant Present in the following documents:
  • Main text
View BVdb publication page