APP c.1033+677A>G

Variant ID: 21-27371653-T-C

NM_000484.3(APP):c.1033+677A>G

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:

An Intron 7 Polymorphism in APP Affects the Age of Onset of Dementia in Down Syndrome.

International Journal Of Alzheimer'S Disease
Jones, Emma L EL; Ballard, Clive G CG; Prasher, Vee P VP; Arno, Matthew M; Tyrer, Stephen S; Moore, Brian B; Hanney, Maria Luisa ML
Publication Date: 2010-12-20

Variant appearance in text: rs9982544
PubMed Link: 21197396
Variant Present in the following documents:
  • Main text
  • IJAD2011-929102.pdf
View BVdb publication page