CETP c.659-21G>A

Variant ID: 16-57005883-G-A

NM_000078.2(CETP):c.659-21G>A

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Multiplexed Targeted Resequencing Identifies Coding and Regulatory Variation Underlying Phenotypic Extremes of High-Density Lipoprotein Cholesterol in Humans.

Circulation. Genomic And Precision Medicine
Khetarpal, Sumeet A SA; Babb, Paul L PL; Zhao, Wei W; Hancock-Cerutti, William F WF; Brown, Christopher D CD; Rader, Daniel J DJ; Voight, Benjamin F BF
Publication Date: 2018-07

Variant appearance in text: rs374409989
PubMed Link: 29987113
Variant Present in the following documents:
  • Main text
View BVdb publication page