COMT c.-91-1825A>T

Variant ID: 22-19946897-A-T

NM_000754.3(COMT):c.-91-1825A>T

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: rs56104268
PubMed Link: 30420678
Variant Present in the following documents:
  • Main text
  • 41431_2018_Article_300.pdf
View BVdb publication page