LPL c.56C>G ;(p.T19S)

Variant ID: 8-19797007-C-G

NM_000237.2(LPL):c.56C>G;(p.T19S)

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Screening program for familial hyperchylomicronemia syndrome detection: Experience of a university health system.

Archives Of Endocrinology And Metabolism
Masson, Walter W; Barbagelata, Leandro L; Fleitas, Milagros M; Herzkovich, Nicole N; Kerschner, Eliana E; Rossi, Emiliano E; Siniawski, Daniel D; Ami, MarĂ­a V MV; Nogueira, Juan P JP
Publication Date: 2023-02-07

Variant appearance in text: LPL: 56C>G
PubMed Link: 36748937
Variant Present in the following documents:
  • 2359-4292-aem-67-03-0408.pdf
View BVdb publication page



New insights into apolipoprotein A5 in controlling lipoprotein metabolism in obesity and the metabolic syndrome patients.

Lipids In Health And Disease
Su, Xin X; Kong, Yi Y; Peng, Dao-Quan DQ
Publication Date: 2018-07-27

Variant appearance in text: LPL: 56C>G
PubMed Link: 30053818
Variant Present in the following documents:
  • Main text
  • 12944_2018_Article_833.pdf
View BVdb publication page



Genetic variants in Apolipoprotein AV alter triglyceride concentrations in pregnancy.

Lipids In Health And Disease
Ward, Kirsten J KJ; Shields, Beverley B; Knight, Beatrice B; Salzmann, Maurice B MB; Hattersley, Andrew T AT; Frayling, Timothy M TM
Publication Date: 2003-11-05

Variant appearance in text: LPL: 56C>G
PubMed Link: 14613578
Variant Present in the following documents:
  • Main text
  • 1476-511X-2-9.pdf
View BVdb publication page