APP c.1091-4873G>A

Variant ID: 21-27359663-C-T

NM_000484.3(APP):c.1091-4873G>A

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Brain Region-Dependent Alternative Splicing of Alzheimer Disease (AD)-Risk Genes Is Associated With Neuropathological Features in AD.

International Neurourology Journal
Kim, Sara S; Han, Seonggyun S; Cho, Soo-Ah SA; Nho, Kwangsik K; Koh, Insong I; Lee, Younghee Y
Publication Date: 2022-11

Variant appearance in text: rs117650267
PubMed Link: 36503215
Variant Present in the following documents:
  • Main text
  • inj-2244258-129.pdf
View BVdb publication page



Role of common and rare APP DNA sequence variants in Alzheimer disease.

Neurology
Hooli, B V BV; Mohapatra, G G; Mattheisen, M M; Parrado, A R AR; Roehr, J T JT; Shen, Y Y; Gusella, J F JF; Moir, R R; Saunders, A J AJ; Lange, C C; Tanzi, R E RE; Bertram, L L
Publication Date: 2012-04-17

Variant appearance in text: rs117650267
PubMed Link: 22491860
Variant Present in the following documents:
  • Main text
View BVdb publication page