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ESR1 c.1096+14048T>C
Variant ID: 6-152279691-T-C
NM_000125.3(
ESR1
):c.1096+14048T>C
This variant was identified in 1 publication
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
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: rs7748205
PubMed Link:
21658281
Variant Present in the following documents:
Main text
1471-2261-11-29.pdf
View BVdb publication page