APP c.659G>A ;(p.G220E)

Variant ID: 21-27423319-C-T

NM_000484.3(APP):c.659G>A;(p.G220E)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Rare variants in APP, PSEN1 and PSEN2 increase risk for AD in late-onset Alzheimer's disease families.

Plos One
Cruchaga, Carlos C; Haller, Gabe G; Chakraverty, Sumitra S; Mayo, Kevin K; Vallania, Francesco L M FL; Mitra, Robi D RD; Faber, Kelley K; Williamson, Jennifer J; Bird, Tom T; Diaz-Arrastia, Ramon R; Foroud, Tatiana M TM; Boeve, Bradley F BF; Graff-Radford, Neill R NR; St Jean, Pamela P; Lawson, Michael M; Ehm, Margaret G MG; Mayeux, Richard R; Goate, Alison M AM; ,
Publication Date: 2012

Variant appearance in text: APP: G220E
PubMed Link: 22312439
Variant Present in the following documents:
  • Main text
  • pone.0031039.pdf
View BVdb publication page