LDLR c.1586+493C>T

Variant ID: 19-11224931-C-T

NM_000527.4(LDLR):c.1586+493C>T

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Whole genome sequencing identifies high-impact variants in well-known pharmacogenomic genes.

The Pharmacogenomics Journal
Choi, Jihoon J; Tantisira, Kelan G KG; Duan, Qing Ling QL
Publication Date: 2019-04

Variant appearance in text: rs2738444
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Multiple genetic imaging study of the association between cholesterol metabolism and brain functional alterations in individuals with risk factors for Alzheimer's disease.

Oncotarget
Bai, Feng F; Yuan, Yonggui Y; Shi, Yongmei Y; Zhang, Zhijun Z
Publication Date: 2016-03-29

Variant appearance in text: rs2738444
PubMed Link: 26985771
Variant Present in the following documents:
  • Main text
  • oncotarget-07-15315.pdf
View BVdb publication page



Association study of candidate gene polymorphisms with amnestic mild cognitive impairment in a Chinese population.

Plos One
Liu, Xiaoyan X; Yue, Chunxian C; Xu, Zhi Z; Shu, Hao H; Pu, Mengjia M; Yu, Hui H; Shi, Yongmei Y; Zhuang, Liying L; Xu, Xiaohui X; Zhang, Zhijun Z
Publication Date: 2012

Variant appearance in text: rs2738444
PubMed Link: 22911757
Variant Present in the following documents:
  • Main text
  • pone.0041198.pdf
View BVdb publication page