LCAT c.368G>A ;(p.R123H)

Variant ID: 16-67976823-C-T

NM_000229.1(LCAT):c.368G>A;(p.R123H)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Association of Genetically Predicted Lipid Levels With the Extent of Coronary Atherosclerosis in Icelandic Adults.

Jama Cardiology
Björnsson, Eythór E; Thorleifsson, Guðmar G; Helgadóttir, Anna A; Guðnason, Thórarinn T; Guðbjartsson, Tómas T; Andersen, Karl K; Grétarsdóttir, Sólveig S; Ólafsson, Ísleifur Í; Tragante, Vinicius V; Ólafsson, Ólafur Hreiðar ÓH; Jónsdóttir, Birna B; Eyjólfsson, Guðmundur I GI; Sigurðardóttir, Ólöf Ó; Thorgeirsson, Guðmundur G; Guðbjartsson, Daníel F DF; Thorsteinsdóttir, Unnur U; Hólm, Hilma H; Stefánsson, Kári K
Publication Date: 2020-01-01

Variant appearance in text: rs199717050
PubMed Link: 31746962
Variant Present in the following documents:
  • jamacardiol-5-13-s001.pdf
View BVdb publication page



Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study.

Plos Genetics
Davis, James P JP; Huyghe, Jeroen R JR; Locke, Adam E AE; Jackson, Anne U AU; Sim, Xueling X; Stringham, Heather M HM; Teslovich, Tanya M TM; Welch, Ryan P RP; Fuchsberger, Christian C; Narisu, Narisu N; Chines, Peter S PS; Kangas, Antti J AJ; Soininen, Pasi P; Ala-Korpela, Mika M; Kuusisto, Johanna J; Collins, Francis S FS; Laakso, Markku M; Boehnke, Michael M; Mohlke, Karen L KL
Publication Date: 2017-10

Variant appearance in text: LCAT: Arg123His; rs199717050
PubMed Link: 29084231
Variant Present in the following documents:
  • Main text
  • pgen.1007079.pdf
View BVdb publication page