SORT1 c.963+1182A>G

Variant ID: 1-109887191-T-C

NM_002959.5(SORT1):c.963+1182A>G

This variant was identified in 5 publications

View GRCh38 version.




Publications:


Low LDL cholesterol, PCSK9 and HMGCR genetic variation, and risk of Alzheimer's disease and Parkinson's disease: Mendelian randomisation study.

Bmj (Clinical Research Ed.)
Benn, Marianne M; Nordestgaard, Børge G BG; Frikke-Schmidt, Ruth R; Tybjærg-Hansen, Anne A
Publication Date: 2017-04-24

Variant appearance in text: rs4970843
PubMed Link: 28438747
Variant Present in the following documents:
  • benm033277.ww1.pdf
View BVdb publication page



A novel method for testing association of multiple genetic markers with a multinomial trait.

Proceedings. American Statistical Association. Annual Meeting
Kwon, Soonil S; Goodarzi, Mark O MO; Taylor, Kent D KD; Cui, Jinrui J; Chen, Y-D Ida YD; Rotter, Jerome I JI; Hsueh, Willa W; Guo, Xiuqing X
Publication Date: 2010

Variant appearance in text: rs4970843
PubMed Link: 26005397
Variant Present in the following documents:
  • Main text
View BVdb publication page



A systematic heritability analysis of the human whole blood transcriptome.

Human Genetics
Huan, Tianxiao T; Liu, Chunyu C; Joehanes, Roby R; Zhang, Xiaoling X; Chen, Brian H BH; Johnson, Andrew D AD; Yao, Chen C; Courchesne, Paul P; O'Donnell, Christopher J CJ; Munson, Peter J PJ; Levy, Daniel D
Publication Date: 2015-03

Variant appearance in text: rs4970843
PubMed Link: 25585846
Variant Present in the following documents:
  • Main text
View BVdb publication page



Serum cholesterol and variant in cholesterol-related gene CETP predict white matter microstructure.

Neurobiology Of Aging
Warstadt, Nicholus M NM; Dennis, Emily L EL; Jahanshad, Neda N; Kohannim, Omid O; Nir, Talia M TM; McMahon, Katie L KL; de Zubicaray, Greig I GI; Montgomery, Grant W GW; Henders, Anjali K AK; Martin, Nicholas G NG; Whitfield, John B JB; Jack, Clifford R CR; Bernstein, Matt A MA; Weiner, Michael W MW; Toga, Arthur W AW; Wright, Margaret J MJ; Thompson, Paul M PM; ,
Publication Date: 2014-11

Variant appearance in text: rs4970843
PubMed Link: 24997672
Variant Present in the following documents:
  • Main text
View BVdb publication page



Analysis of recently identified dyslipidemia alleles reveals two loci that contribute to risk for carotid artery disease.

Lipids In Health And Disease
Ronald, James J; Rajagopalan, Ramakrishnan R; Ranchalis, Jane E JE; Marshall, Julieann K JK; Hatsukami, Thomas S TS; Heagerty, Patrick J PJ; Jarvik, Gail P GP
Publication Date: 2009-12-01

Variant appearance in text: rs4970843
PubMed Link: 19951432
Variant Present in the following documents:
  • Main text
  • 1476-511X-8-52.pdf
View BVdb publication page