APP c.57+10810T>C

Variant ID: 21-27532072-A-G

NM_000484.3(APP):c.57+10810T>C

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Family-based association analyses of imputed genotypes reveal genome-wide significant association of Alzheimer's disease with OSBPL6, PTPRG, and PDCL3.

Molecular Psychiatry
Herold, C C; Hooli, B V BV; Mullin, K K; Liu, T T; Roehr, J T JT; Mattheisen, M M; Parrado, A R AR; Bertram, L L; Lange, C C; Tanzi, R E RE
Publication Date: 2016-11

Variant appearance in text: rs141145244
PubMed Link: 26830138
Variant Present in the following documents:
  • Main text
  • nihms-743432.pdf
View BVdb publication page