Variant ID: 1-55527222-A-T

NM_174936.3(PCSK9):c.1856A>T;(p.Q619L)

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: rs28362277
PubMed Link: 30779729
Variant Present in the following documents:
  • Main text
View BVdb publication page