Bibliome.ai browser hg19
Search
About
Stats
FAQ
APOE c.334T>C ;(p.S112P)
Variant ID: 19-45411887-T-C
NM_000041.2(
APOE
):c.334T>C;(p.S112P)
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:
Increase of serum uric acid levels associated with APOE ε2 haplotype: a clinico-genetic investigation and in vivo approach.
Human Cell
Ogura, Masatsune M; Toyoda, Yu Y; Sakiyama, Masayuki M; Kawamura, Yusuke Y; Nakayama, Akiyoshi A; Yamanashi, Yoshihide Y; Takada, Tappei T; Shimizu, Seiko S; Higashino, Toshihide T; Nakajima, Mayuko M; Naito, Mariko M; Hishida, Asahi A; Kawai, Sayo S; Okada, Rieko R; Sasaki, Makoto M; Ayaori, Makoto M; Suzuki, Hiroshi H; Takata, Koki K; Ikewaki, Katsunori K; Harada-Shiba, Mariko M; Shinomiya, Nariyoshi N; Matsuo, Hirotaka H
Publication Date: 2021-11
Variant appearance in text: APOE: 334T>C
PubMed Link:
34532841
Variant Present in the following documents:
Main text
13577_2021_Article_609.pdf
View BVdb publication page
Apolipoprotein E Gene Polymorphism, Glycated Hemoglobin, and Peripheral Arterial Disease Risk in Chinese Type 2 Diabetic Patients.
Disease Markers
Hu, Yujing Y; Ling, Tinghuan T; Yu, Min M; Bai, Yang Y; Feng, Tongbao T; Zhang, Ping P; Wang, Yan Y
Publication Date: 2020
Variant appearance in text: APOE: 334T>C
PubMed Link:
32211081
Variant Present in the following documents:
DM2020-6040525.pdf
View BVdb publication page