Bibliome.ai browser hg19
Search
About
Stats
FAQ
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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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