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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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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