APOC3 c.180-334C>A

Variant ID: 11-116703146-C-A

NM_000040.1(APOC3):c.180-334C>A

This variant was identified in 5 publications

View GRCh38 version.




Publications:


Spotlight on very-low-density lipoprotein as a driver of cardiometabolic disorders: Implications for disease progression and mechanistic insights.

Frontiers In Cardiovascular Medicine
Lee, Hsiang-Chun HC; Akhmedov, Alexander A; Chen, Chu-Huang CH
Publication Date: 2022

Variant appearance in text: rs5130
PubMed Link: 36267630
Variant Present in the following documents:
  • Main text
  • fcvm-09-993633.pdf
View BVdb publication page



Sequence analysis and variant identification at the APOC3 gene locus indicates association of rs5218 with BMI in a sample of Kuwaiti's.

Lipids In Health And Disease
Malalla, Zainab H ZH; Al-Serri, Ahmad E AE; AlAskar, Huda M HM; Al-Kandari, Wafaa Y WY; Al-Bustan, Suzanne A SA
Publication Date: 2019-12-19

Variant appearance in text: rs5130
PubMed Link: 31856839
Variant Present in the following documents:
  • Main text
  • 12944_2019_Article_1165.pdf
View BVdb publication page



Genetic Evidence Supporting the Role of the Calcium Channel, CACNA1S, in Tooth Cusp and Root Patterning.

Frontiers In Physiology
Laugel-Haushalter, Virginie V; Morkmued, Supawich S; Stoetzel, Corinne C; Geoffroy, Véronique V; Muller, Jean J; Boland, Anne A; Deleuze, Jean-François JF; Chennen, Kirsley K; Pitiphat, Waranuch W; Dollfus, Hélène H; Niederreither, Karen K; Bloch-Zupan, Agnès A; Pungchanchaikul, Patimaporn P
Publication Date: 2018

Variant appearance in text: rs5130
PubMed Link: 30319441
Variant Present in the following documents:
  • Table_6.xlsx, sheet 1
View BVdb publication page



Very low-depth sequencing in a founder population identifies a cardioprotective APOC3 signal missed by genome-wide imputation.

Human Molecular Genetics
Gilly, Arthur A; Ritchie, Graham Rs GR; Southam, Lorraine L; Farmaki, Aliki-Eleni AE; Tsafantakis, Emmanouil E; Dedoussis, George G; Zeggini, Eleftheria E
Publication Date: 2016-06-01

Variant appearance in text: rs5130
PubMed Link: 27146844
Variant Present in the following documents:
  • Main text
  • ddw088.pdf
View BVdb publication page