Varaico: Literature-Extracted Genetic Variants

Gene:APP
Variant:p.G58A
Back to variants list

APP

NM_000484.4:p.G58A

Associated Papers

Biophysical characterization of TREM2 missense variants implicated in neurodegenerative disease.

Pillai J et al.

Computational and Structural Biotechnology Journal, 2025

Defects in the acid phosphatase ACPT cause recessive hypoplastic amelogenesis imperfecta.

Smith CE et al.

European Journal of Human Genetics : Ejhg, 2017

28513613 (PubMed )
Supplement: ejhg201779x2.docx
Select a paper to view details
UCSC Genome Browser·Imprint·Privacy·Terms·Feedback·Email Updates·

Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."