SNF8 c.244+1449C>T

Variant ID: 17-47016837-G-A

NM_007241.2(SNF8):c.244+1449C>T

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Genetic Susceptibility Loci for Cardiovascular Disease and Their Impact on Atherosclerotic Plaques.

Circulation. Genomic And Precision Medicine
van der Laan, Sander W SW; Siemelink, Marten A MA; Haitjema, Saskia S; Foroughi Asl, Hassan H; Perisic, Ljubica L; Mokry, Michal M; van Setten, Jessica J; Malik, Rainer R; Dichgans, Martin M; Worrall, Bradford B BB; , ; Samani, Nilesh J NJ; Schunkert, Heribert H; Erdmann, Jeanette J; Hedin, Ulf U; Paulsson-Berne, Gabrielle G; Björkegrenn, Johan L M JLM; de Borst, Gert J GJ; Asselbergs, Folkert W FW; den Ruijter, Folkert W FW; de Bakker, Paul I W PIW; Pasterkamp, Gerard G
Publication Date: 2018-09

Variant appearance in text: rs12232531
PubMed Link: 30354329
Variant Present in the following documents:
  • hcg-11-e002115-s001.pdf
View BVdb publication page