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APP c.57+11615A>G
Variant ID: 21-27531267-T-C
NM_000484.3(
APP
):c.57+11615A>G
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Association of APP gene polymorphisms and promoter methylation with essential hypertension in Guizhou: a case-control study.
Human Genomics
Li, Ruichao R; Song, Juhui J; Zhao, Ansu A; Diao, Xiaoyan X; Zhang, Ting T; Qi, Xiaolan X; Guan, Zhizhong Z; An, Yu Y; Ren, Lingyan L; Wang, Chanjuan C; He, Yan Y
Publication Date: 2023-03-20
Variant appearance in text: rs368196
PubMed Link:
36941702
Variant Present in the following documents:
Main text
40246_2023_Article_462.pdf
View BVdb publication page
Implication of the APP Gene in Intellectual Abilities.
Journal Of Alzheimer'S Disease : Jad
Myrum, Craig C; Nikolaienko, Oleksii O; Bramham, Clive R CR; Haavik, Jan J; Zayats, Tetyana T
Publication Date: 2017
Variant appearance in text: rs368196
PubMed Link:
28671113
Variant Present in the following documents:
Main text
jad-59-jad170049.pdf
View BVdb publication page