Variant ID: 1-55521784-G-C

NM_174936.3(PCSK9):c.918G>C;(p.R306S)

This variant was identified in 3 publications

View GRCh38 version.




Publications:


PCSK9 Gene E670G Polymorphism and Coronary Artery Disease: An Updated Meta-Analysis of 5,484 Subjects.

Frontiers In Cardiovascular Medicine
Li, Yan-Yan YY; Wang, Hui H; Yang, Xin-Xing XX; Geng, Hong-Yu HY; Gong, Ge G; Lu, Xin-Zheng XZ
Publication Date: 2020

Variant appearance in text: PCSK9: R306S
PubMed Link: 33244470
Variant Present in the following documents:
  • Main text
View BVdb publication page



Current Status of Familial Hypercholesterolemia in China: A Need for Patient FH Registry Systems.

Frontiers In Physiology
Chen, Peipei P; Chen, Xi X; Zhang, Shuyang S
Publication Date: 2019

Variant appearance in text: PCSK9: R306S
PubMed Link: 30949068
Variant Present in the following documents:
  • Main text
View BVdb publication page



The distribution and characteristics of LDL receptor mutations in China: A systematic review.

Scientific Reports
Jiang, Long L; Sun, Li-Yuan LY; Dai, Yan-Fang YF; Yang, Shi-Wei SW; Zhang, Feng F; Wang, Lu-Ya LY
Publication Date: 2015-11-26

Variant appearance in text: PCSK9: R306S
PubMed Link: 26608663
Variant Present in the following documents:
  • Main text
View BVdb publication page