EPHB2 c.62-13493C>T

Variant ID: 1-23094421-C-T

NM_017449.3(EPHB2):c.62-13493C>T

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Linkage analysis of multiplex Caribbean Hispanic families loaded for unexplained early-onset cases identifies novel Alzheimer's disease loci.

Alzheimer'S & Dementia (Amsterdam, Netherlands)
Cheng, Rong R; Tang, Min M; Martinez, Izri I; Ayodele, Temitope T; Baez, Penelope P; Reyes-Dumeyer, Dolly D; Lantigua, Rafael R; Medrano, Martin M; Jimenez-Velazquez, Ivonne I; Lee, Joseph H JH; Beecham, Gary W GW; Reitz, Christiane C
Publication Date: 2018

Variant appearance in text: rs4654814
PubMed Link: 30406174
Variant Present in the following documents:
  • Main text
  • main.pdf
View BVdb publication page



Evaluation of potential novel variations and their interactions related to bipolar disorders: analysis of genome-wide association study data.

Neuropsychiatric Disease And Treatment
Acikel, Cengizhan C; Aydin Son, Yesim Y; Celik, Cemil C; Gul, Husamettin H
Publication Date: 2016

Variant appearance in text: rs4654814
PubMed Link: 27920536
Variant Present in the following documents:
  • Main text
  • ndt-12-2997.pdf
View BVdb publication page