APOB c.2816+374C>A

Variant ID: 2-21245329-G-T

NM_000384.2(APOB):c.2816+374C>A

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Harnessing publicly available genetic data to prioritize lipid modifying therapeutic targets for prevention of coronary heart disease based on dysglycemic risk.

Human Genetics
Tragante, Vinicius V; Asselbergs, Folkert W FW; Swerdlow, Daniel I DI; Palmer, Tom M TM; Moore, Jason H JH; de Bakker, Paul I W PIW; Keating, Brendan J BJ; Holmes, Michael V MV
Publication Date: 2016-05

Variant appearance in text: rs3791980
PubMed Link: 26946290
Variant Present in the following documents:
  • Main text
  • 439_2016_Article_1647.pdf
View BVdb publication page



Polymorphisms in ApoB gene are associated with risk of myocardial infarction and serum ApoB levels in a Chinese population.

International Journal Of Clinical And Experimental Medicine
Liu, Changqing C; Yang, Jing J; Han, Wei W; Zhang, Qi Q; Shang, Xiaoming X; Li, Xia X; Lu, Feng F; Liu, Xiaokun X
Publication Date: 2015

Variant appearance in text: rs3791980
PubMed Link: 26629186
Variant Present in the following documents:
  • Main text
View BVdb publication page



Low-density lipoprotein cholesterol, apolipoprotein B, and risk of coronary heart disease: from familial hyperlipidemia to genomics.

Biological Research For Nursing
Imes, Christopher C CC; Austin, Melissa A MA
Publication Date: 2013-07

Variant appearance in text: rs3791980
PubMed Link: 22531366
Variant Present in the following documents:
  • Main text
View BVdb publication page