DBP c.169G>A ;(p.A57T)

Variant ID: 19-49139218-C-T

NM_001352.3(DBP):c.169G>A;(p.A57T)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


PCSK9 variation and association with blood pressure in African Americans: preliminary findings from the HyperGEN and REGARDS studies.

Frontiers In Genetics
Tran, Ngan T NT; Aslibekyan, Stella S; Tiwari, Hemant K HK; Zhi, Degui D; Sung, Yun Ju YJ; Hunt, Steven C SC; Rao, D C DC; Broeckel, Ulrich U; Judd, Suzanne E SE; Muntner, Paul P; Kent, Shia T ST; Arnett, Donna K DK; Irvin, Marguerite R MR
Publication Date: 2015

Variant appearance in text: DBP: 169G>A
PubMed Link: 25904937
Variant Present in the following documents:
  • Main text
  • fgene-06-00136.pdf
View BVdb publication page