Bibliome.ai browser hg19
Search
About
Stats
FAQ
PSEN1 c.*313C>T
Variant ID: 14-73686310-C-T
NM_000021.3(
PSEN1
):c.*313C>T
This variant was identified in 3 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Genome-Wide Association Study of Brain Connectivity Changes for Alzheimer's Disease.
Scientific Reports
Elsheikh, Samar S M SSM; Chimusa, Emile R ER; Mulder, Nicola J NJ; Crimi, Alessandro A
Publication Date: 2020-01-29
Variant appearance in text: rs362384
PubMed Link:
31996736
Variant Present in the following documents:
Main text
41598_2020_Article_58291.pdf
View BVdb publication page
PGG.SNV: understanding the evolutionary and medical implications of human single nucleotide variations in diverse populations.
Genome Biology
Zhang, Chao C; Gao, Yang Y; Ning, Zhilin Z; Lu, Yan Y; Zhang, Xiaoxi X; Liu, Jiaojiao J; Xie, Bo B; Xue, Zhe Z; Wang, Xiaoji X; Yuan, Kai K; Ge, Xueling X; Pan, Yuwen Y; Liu, Chang C; Tian, Lei L; Wang, Yuchen Y; Lu, Dongsheng D; Hoh, Boon-Peng BP; Xu, Shuhua S
Publication Date: 2019-10-22
Variant appearance in text: rs362384
PubMed Link:
31640808
Variant Present in the following documents:
13059_2019_1838_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page
Canonical correlation analysis for RNA-seq co-expression networks.
Nucleic Acids Research
Hong, Shengjun S; Chen, Xiangning X; Jin, Li L; Xiong, Momiao M
Publication Date: 2013-04
Variant appearance in text: rs362384
PubMed Link:
23460206
Variant Present in the following documents:
Main text
gkt145.pdf
View BVdb publication page