Variant ID: 1-55529828-C-T

NM_174936.3(PCSK9):c.*571C>T

This variant was identified in 7 publications

View GRCh38 version.




Publications:


Genome-Wide Association of Proprotein Convertase Subtilisin/Kexin Type 9 Plasma Levels in the ELSA-Brasil Study.

Frontiers In Genetics
Bensenor, Isabela I; Padilha, Kallyandra K; Lima, Isabella Ramos IR; Santos, Raul Dias RD; Lambert, Gilles G; Ramin-Mangata, St├ęphane S; Bittencourt, Marcio S MS; Goulart, Alessandra C AC; Santos, Itamar S IS; Mill, Jose G JG; Krieger, Jose E JE; Lotufo, Paulo A PA; Pereira, Alexandre C AC
Publication Date: 2021

Variant appearance in text: rs662145
PubMed Link: 34659352
Variant Present in the following documents:
  • Main text
  • fgene-12-728526.pdf
View BVdb publication page



Association of Lipoprotein (a) variants with risk of cardiovascular disease: a Mendelian randomization study.

Lipids In Health And Disease
Xia, Juan J; Guo, Chunyue C; Liu, Kuo K; Xie, Yunyi Y; Cao, Han H; Peng, Wenjuan W; Sun, Yanyan Y; Liu, Xiaohui X; Li, Bingxiao B; Zhang, Ling L
Publication Date: 2021-06-01

Variant appearance in text: rs662145
PubMed Link: 34074296
Variant Present in the following documents:
  • Main text
View BVdb publication page



Susceptibility of ApoB and PCSK9 Genetic Polymorphisms to Diabetic Kidney Disease Among Chinese Diabetic Patients.

Frontiers In Medicine
Ma, Liang L; Wang, Shaoting S; Zhao, Hailing H; Yu, Meijie M; Deng, Xiangling X; Jiang, Yongwei Y; Cao, Yongtong Y; Li, Ping P; Niu, Wenquan W
Publication Date: 2021

Variant appearance in text: rs662145
PubMed Link: 33889589
Variant Present in the following documents:
  • Main text
  • fmed-08-659188.pdf
View BVdb publication page



Proprotein Convertase Subtilisin/Kexin Type 9 (PCSK9) in the Brain and Relevance for Neuropsychiatric Disorders.

Frontiers In Neuroscience
O'Connell, Emma M EM; Lohoff, Falk W FW
Publication Date: 2020

Variant appearance in text: rs662145
PubMed Link: 32595449
Variant Present in the following documents:
  • Main text
View BVdb publication page



Polymorphisms in PCSK9, LDLR, BCMO1, SLC12A3, and KCNJ1 are Associated with Serum Lipid Profile in Chinese Han Population.

International Journal Of Environmental Research And Public Health
Li, Zheng Z; Zhao, Tianyu T; Tan, Xiaohua X; Lei, Song S; Huang, Liu L; Yang, Lei L
Publication Date: 2019-09-02

Variant appearance in text: rs662145
PubMed Link: 31480784
Variant Present in the following documents:
  • Main text
View BVdb publication page



The dual behavior of PCSK9 in the regulation of apoptosis is crucial in Alzheimer's disease progression (Review).

Biomedical Reports
Wu, Qi Q; Tang, Zhi-Han ZH; Peng, Juan J; Liao, Ling L; Pan, Li-Hong LH; Wu, Chun-Yan CY; Jiang, Zhi-Sheng ZS; Wang, Gui-Xue GX; Liu, Lu-Shan LS
Publication Date: 2014-03

Variant appearance in text: rs662145
PubMed Link: 24649090
Variant Present in the following documents:
  • Main text
View BVdb publication page



PCSK9 SNP rs11591147 is associated with low cholesterol levels but not with cognitive performance or noncardiovascular clinical events in an elderly population.

Journal Of Lipid Research
Postmus, Iris I; Trompet, Stella S; de Craen, Anton J M AJ; Buckley, Brendan M BM; Ford, Ian I; Stott, David J DJ; Sattar, Naveed N; Slagboom, P Eline PE; Westendorp, Rudi G J RG; Jukema, J Wouter JW
Publication Date: 2013-02

Variant appearance in text: rs662145
PubMed Link: 23300213
Variant Present in the following documents:
  • Main text
View BVdb publication page