Variant ID: 1-55529153-C-G

NM_174936.3(PCSK9):c.1975C>G;(p.R659G)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Identifying individual risk rare variants using protein structure guided local tests (POINT).

Plos Computational Biology
Marceau West, Rachel R; Lu, Wenbin W; Rotroff, Daniel M DM; Kuenemann, Melaine A MA; Chang, Sheng-Mao SM; Wu, Michael C MC; Wagner, Michael J MJ; Buse, John B JB; Motsinger-Reif, Alison A AA; Fourches, Denis D; Tzeng, Jung-Ying JY
Publication Date: 2019-02

Variant appearance in text: rs147182054
PubMed Link: 30779729
Variant Present in the following documents:
  • Main text
View BVdb publication page