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ESR1 c.1096+14024G>T
Variant ID: 6-152279667-G-T
NM_000125.3(
ESR1
):c.1096+14024G>T
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Usefulness of Single Nucleotide Polymorphisms as Predictors of Sudden Cardiac Death.
The American Journal Of Cardiology
Tamariz, Leonardo L; Balda, Javier J; Pareja, Dennise D; Palacio, Ana A; Myerburg, Robert J RJ; Conway, Douglas D; Davis, Lea L; Goldberger, Jeffrey J JJ
Publication Date: 2019-06-15
Variant appearance in text: rs3003922
PubMed Link:
31053292
Variant Present in the following documents:
Main text
View BVdb publication page
GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease.
Bmc Cardiovascular Disorders
Aouizerat, Bradley E BE; Vittinghoff, Eric E; Musone, Stacy L SL; Pawlikowska, Ludmila L; Kwok, Pui-Yan PY; Olgin, Jeffrey E JE; Tseng, Zian H ZH
Publication Date: 2011-06-10
Variant appearance in text: rs3003922
PubMed Link:
21658281
Variant Present in the following documents:
Main text
1471-2261-11-29.pdf
View BVdb publication page