PLPP3 c.139+8194G>T

Variant ID: 1-57036357-C-A

NM_003713.4(PLPP3):c.139+8194G>T

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Study of the association of 17 lipid-related gene polymorphisms with coronary heart disease.

Anatolian Journal Of Cardiology
Wu, Nan N; Liu, Guili G; Huang, Yi Y; Liao, Qi Q; Han, Liyuan L; Ye, Huandan H; Duan, Shiwei S; Chen, Xiaomin X
Publication Date: 2018-06

Variant appearance in text: rs12566304
PubMed Link: 29848931
Variant Present in the following documents:
  • Main text
  • AJC-19-360.pdf
View BVdb publication page



Association between PPAP2B gene polymorphisms and coronary heart disease susceptibility in Chinese Han males and females.

Oncotarget
Sun, Yu-Xiao YX; Gao, Chuan-Yu CY; Lu, Yang Y; Fu, Xin X; Jia, Jun-Ge JG; Zhao, Yu-Jie YJ; Li, Lian-Dong LD; Dui, Hong-Zhi HZ; Zhang, Xing-Yu XY; Li, Zhi-Ying ZY; Lei, Lei L; Zhang, Wei-Feng WF; Yuan, Yi-Qiang YQ
Publication Date: 2017-02-21

Variant appearance in text: rs12566304
PubMed Link: 28061459
Variant Present in the following documents:
  • Main text
  • oncotarget-08-13166.pdf
View BVdb publication page



Identification of risk and age-at-onset genes on chromosome 1p in Parkinson disease.

American Journal Of Human Genetics
Oliveira, Sofia A SA; Li, Yi-Ju YJ; Noureddine, Maher A MA; Zuchner, Stephan S; Qin, Xuejun X; Pericak-Vance, Margaret A MA; Vance, Jeffery M JM
Publication Date: 2005-08

Variant appearance in text: rs12566304
PubMed Link: 15986317
Variant Present in the following documents:
  • Main text
View BVdb publication page