APP c.58-16197A>C

Variant ID: 21-27500660-T-G

NM_000484.3(APP):c.58-16197A>C

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Association study of selenium-related gene polymorphisms with geriatric depression in China.

Medicine
Liu, Yu Y; Wang, Liqun L; Wang, Zhizhong Z; He, Shulan S
Publication Date: 2023-04-25

Variant appearance in text: rs2830072
PubMed Link: 37115082
Variant Present in the following documents:
  • Main text
  • medi-102-e33594.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: rs2830072
PubMed Link: 28671113
Variant Present in the following documents:
  • Main text
  • jad-59-jad170049.pdf
View BVdb publication page



Genetic variation in PCDH11X is associated with susceptibility to late-onset Alzheimer's disease.

Nature Genetics
Carrasquillo, Minerva M MM; Zou, Fanggeng F; Pankratz, V Shane VS; Wilcox, Samantha L SL; Ma, Li L; Walker, Louise P LP; Younkin, Samuel G SG; Younkin, Curtis S CS; Younkin, Linda H LH; Bisceglio, Gina D GD; Ertekin-Taner, Nilufer N; Crook, Julia E JE; Dickson, Dennis W DW; Petersen, Ronald C RC; Graff-Radford, Neill R NR; Younkin, Steven G SG
Publication Date: 2009-02

Variant appearance in text: rs2830072
PubMed Link: 19136949
Variant Present in the following documents:
  • Main text
View BVdb publication page