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APP c.2065-1527C>T
Variant ID: 21-27265707-G-A
NM_000484.3(
APP
):c.2065-1527C>T
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:
Artificial Intelligence-Assisted Identification of Genetic Factors Predisposing High-Risk Individuals to Asymptomatic Heart Failure.
Cells
Yang, Ning-I NI; Yeh, Chi-Hsiao CH; Tsai, Tsung-Hsien TH; Chou, Yi-Ju YJ; Hsu, Paul Wei-Che PW; Li, Chun-Hsien CH; Chan, Yun-Hsuan YH; Kuo, Li-Tang LT; Mao, Chun-Tai CT; Shyu, Yu-Chiau YC; Hung, Ming-Jui MJ; Lai, Chi-Chun CC; Sytwu, Huey-Kang HK; Tsai, Ting-Fen TF
Publication Date: 2021-09-15
Variant appearance in text: rs6516709
PubMed Link:
34572079
Variant Present in the following documents:
Main text
cells-10-02430.pdf
View BVdb publication page