APP c.57+8621A>G

Variant ID: 21-27534261-T-C

NM_000484.3(APP):c.57+8621A>G

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Genome-wide meta-analysis, fine-mapping and integrative prioritization implicate new Alzheimer's disease risk genes.

Nature Genetics
Schwartzentruber, Jeremy J; Cooper, Sarah S; Liu, Jimmy Z JZ; Barrio-Hernandez, Inigo I; Bello, Erica E; Kumasaka, Natsuhiko N; Young, Adam M H AMH; Franklin, Robin J M RJM; Johnson, Toby T; Estrada, Karol K; Gaffney, Daniel J DJ; Beltrao, Pedro P; Bassett, Andrew A
Publication Date: 2021-03

Variant appearance in text: rs4817090
PubMed Link: 33589840
Variant Present in the following documents:
  • EMS118040-supplement-Supplementary_Tables_1_14.xlsx, sheet 2
View BVdb publication page



GWAS on family history of Alzheimer's disease.

Translational Psychiatry
Marioni, Riccardo E RE; Harris, Sarah E SE; Zhang, Qian Q; McRae, Allan F AF; Hagenaars, Saskia P SP; Hill, W David WD; Davies, Gail G; Ritchie, Craig W CW; Gale, Catharine R CR; Starr, John M JM; Goate, Alison M AM; Porteous, David J DJ; Yang, Jian J; Evans, Kathryn L KL; Deary, Ian J IJ; Wray, Naomi R NR; Visscher, Peter M PM
Publication Date: 2018-05-18

Variant appearance in text: rs4817090
PubMed Link: 29777097
Variant Present in the following documents:
  • Main text
  • 41398_2018_Article_150.pdf
View BVdb publication page