APP c.1458+3194T>G

Variant ID: 21-27344189-A-C

NM_000484.3(APP):c.1458+3194T>G

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Examining SNP-SNP interactions and risk of clinical outcomes in colorectal cancer using multifactor dimensionality reduction based methods.

Frontiers In Genetics
Curtis, Aaron A; Yu, Yajun Y; Carey, Megan M; Parfrey, Patrick P; Yilmaz, Yildiz E YE; Savas, Sevtap S
Publication Date: 2022

Variant appearance in text: rs2096488
PubMed Link: 35991579
Variant Present in the following documents:
  • Main text
  • fgene-13-902217.pdf
View BVdb publication page



Genetic alterations of δ-catenin/NPRAP/Neurojungin (CTNND2): functional implications in complex human diseases.

Human Genetics
Lu, Qun Q; Aguilar, Byron J BJ; Li, Mingchuan M; Jiang, Yongguang Y; Chen, Yan-Hua YH
Publication Date: 2016-10

Variant appearance in text: rs2096488
PubMed Link: 27380241
Variant Present in the following documents:
  • Main text
View BVdb publication page



δ-Catenin is genetically and biologically associated with cortical cataract and future Alzheimer-related structural and functional brain changes.

Plos One
Jun, Gyungah G; Moncaster, Juliet A JA; Koutras, Carolina C; Seshadri, Sudha S; Buros, Jacqueline J; McKee, Ann C AC; Levesque, Georges G; Wolf, Philip A PA; St George-Hyslop, Peter P; Goldstein, Lee E LE; Farrer, Lindsay A LA
Publication Date: 2012

Variant appearance in text: rs2096488
PubMed Link: 22984439
Variant Present in the following documents:
  • Main text
  • pone.0043728.pdf
View BVdb publication page