APP c.606G>T ;(p.E202D)

Variant ID: 21-27423372-C-A

NM_000484.3(APP):c.606G>T;(p.E202D)

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

Coding variants in TREM2 increase risk for Alzheimer's disease.

Human Molecular Genetics
Jin, Sheng Chih SC; Benitez, Bruno A BA; Karch, Celeste M CM; Cooper, Breanna B; Skorupa, Tara T; Carrell, David D; Norton, Joanne B JB; Hsu, Simon S; Harari, Oscar O; Cai, Yefei Y; Bertelsen, Sarah S; Goate, Alison M AM; Cruchaga, Carlos C
Publication Date: 2014-11-01

Variant appearance in text: APP: E202D
PubMed Link: 24899047
Variant Present in the following documents:
  • Main text
View BVdb publication page