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RBMS3 c.637+47452T>C
Variant ID: 3-29851932-T-C
NM_001003793.2(
RBMS3
):c.637+47452T>C
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:
A telescope GWAS analysis strategy, based on SNPs-genes-pathways ensamble and on multivariate algorithms, to characterize late onset Alzheimer's disease.
Scientific Reports
Squillario, Margherita M; Abate, Giulia G; Tomasi, Federico F; Tozzo, Veronica V; Barla, Annalisa A; Uberti, Daniela D; ,
Publication Date: 2020-07-21
Variant appearance in text: rs9310917
PubMed Link:
32694537
Variant Present in the following documents:
41598_2020_67699_MOESM1_ESM.pdf
View BVdb publication page