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LDLR c.1845+1544A>G
Variant ID: 19-11229218-A-G
NM_000527.4(
LDLR
):c.1845+1544A>G
This variant was identified in 4 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Inference of a causal relation between low-density lipoprotein cholesterol and hypertension using mendelian randomization analysis.
Clinical Hypertension
Go, Tae-Hwa TH; Kwak, Kyeong Im KI; Jang, Ji-Yun JY; Yu, Minheui M; Kim, Hye Sim HS; Kim, Jang Young JY; Koh, Sang Baek SB; Kang, Dae Ryong DR
Publication Date: 2021-02-26
Variant appearance in text: rs2738452
PubMed Link:
33637130
Variant Present in the following documents:
Main text
40885_2021_Article_162.pdf
View BVdb publication page
Genome-wide landscape establishes novel association signals for metabolic traits in the Arab population.
Human Genetics
Hebbar, Prashantha P; Abubaker, Jehad Ahmed JA; Abu-Farha, Mohamed M; Alsmadi, Osama O; Elkum, Naser N; Alkayal, Fadi F; John, Sumi Elsa SE; Channanath, Arshad A; Iqbal, Rasheeba R; Pitkaniemi, Janne J; Tuomilehto, Jaakko J; Sladek, Robert R; Al-Mulla, Fahd F; Thanaraj, Thangavel Alphonse TA
Publication Date: 2021-03
Variant appearance in text: rs2738452
PubMed Link:
32902719
Variant Present in the following documents:
Main text
View BVdb publication page
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: rs2738452
PubMed Link:
30214008
Variant Present in the following documents:
NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page
Low LDL cholesterol, PCSK9 and HMGCR genetic variation, and risk of Alzheimer's disease and Parkinson's disease: Mendelian randomisation study.
Bmj (Clinical Research Ed.)
Benn, Marianne M; Nordestgaard, Børge G BG; Frikke-Schmidt, Ruth R; Tybjærg-Hansen, Anne A
Publication Date: 2017-04-24
Variant appearance in text: rs2738452
PubMed Link:
28438747
Variant Present in the following documents:
benm033277.ww1.pdf
View BVdb publication page