APP c.57+25805T>A

Variant ID: 21-27517077-A-T

NM_000484.3(APP):c.57+25805T>A

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Association of APP gene polymorphisms and promoter methylation with essential hypertension in Guizhou: a case-control study.

Human Genomics
Li, Ruichao R; Song, Juhui J; Zhao, Ansu A; Diao, Xiaoyan X; Zhang, Ting T; Qi, Xiaolan X; Guan, Zhizhong Z; An, Yu Y; Ren, Lingyan L; Wang, Chanjuan C; He, Yan Y
Publication Date: 2023-03-20

Variant appearance in text: rs467021
PubMed Link: 36941702
Variant Present in the following documents:
  • Main text
  • 40246_2023_Article_462.pdf
View BVdb publication page



Implication of the APP Gene in Intellectual Abilities.

Journal Of Alzheimer'S Disease : Jad
Myrum, Craig C; Nikolaienko, Oleksii O; Bramham, Clive R CR; Haavik, Jan J; Zayats, Tetyana T
Publication Date: 2017

Variant appearance in text: rs467021
PubMed Link: 28671113
Variant Present in the following documents:
  • Main text
  • jad-59-jad170049.pdf
View BVdb publication page