LRP1B c.1014-42068T>A

Variant ID: 2-141861910-A-T

NM_018557.2(LRP1B):c.1014-42068T>A

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Genetic variation in the Estonian population: pharmacogenomics study of adverse drug effects using electronic health records.

European Journal Of Human Genetics : Ejhg
Tasa, Tõnis T; Krebs, Kristi K; Kals, Mart M; Mägi, Reedik R; Lauschke, Volker M VM; Haller, Toomas T; Puurand, Tarmo T; Remm, Maido M; Esko, Tõnu T; Metspalu, Andres A; Vilo, Jaak J; Milani, Lili L
Publication Date: 2019-03

Variant appearance in text: rs1882642
PubMed Link: 30420678
Variant Present in the following documents:
  • Main text
  • 41431_2018_Article_300.pdf
View BVdb publication page