APP c.356-2592G>T

Variant ID: 21-27428256-C-A

NM_000484.3(APP):c.356-2592G>T

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Genetic Variability in the Iron Homeostasis Pathway and Patient Outcomes After Aneurysmal Subarachnoid Hemorrhage.

Neurocritical Care
Heinsberg, Lacey W LW; Alexander, Sheila A SA; Crago, Elizabeth A EA; Minster, Ryan L RL; Poloyac, Samuel M SM; Weeks, Daniel E DE; Conley, Yvette P YP
Publication Date: 2020-12

Variant appearance in text: rs3991
PubMed Link: 32246437
Variant Present in the following documents:
  • Main text
View BVdb publication page



Candidate gene analysis for Alzheimer's disease in adults with Down syndrome.

Neurobiology Of Aging
Lee, Joseph H JH; Lee, Annie J AJ; Dang, Lam-Ha LH; Pang, Deborah D; Kisselev, Sergey S; Krinsky-McHale, Sharon J SJ; Zigman, Warren B WB; Luchsinger, José A JA; Silverman, Wayne W; Tycko, Benjamin B; Clark, Lorraine N LN; Schupf, Nicole N
Publication Date: 2017-08

Variant appearance in text: rs3991
PubMed Link: 28554490
Variant Present in the following documents:
  • Main text
View BVdb publication page



APOE and AβPP gene variation in cortical and cerebrovascular amyloid-β pathology and Alzheimer's disease: a population-based analysis.

Journal Of Alzheimer'S Disease : Jad
Peuralinna, Terhi T; Tanskanen, Maarit M; Mäkelä, Mira M; Polvikoski, Tuomo T; Paetau, Anders A; Kalimo, Hannu H; Sulkava, Raimo R; Hardy, John J; Lai, Shiao-Lin SL; Arepalli, Sampath S; Hernandez, Dena D; Traynor, Bryan J BJ; Singleton, Andrew A; Tienari, Pentti J PJ; Myllykangas, Liisa L
Publication Date: 2011

Variant appearance in text: rs3991
PubMed Link: 21654062
Variant Present in the following documents:
  • Main text
View BVdb publication page