Bibliome.ai browser hg19
Search
About
Stats
FAQ
CHI3L2 c.736-958G>A
Variant ID: 1-111780414-G-A
NM_004000.2(
CHI3L2
):c.736-958G>A
This variant was identified in 4 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
MAGPEL: an autoMated pipeline for inferring vAriant-driven Gene PanEls from the full-length biomedical literature.
Scientific Reports
Saberian, Nafiseh N; Shafi, Adib A; Peyvandipour, Azam A; Draghici, Sorin S
Publication Date: 2020-07-23
Variant appearance in text: rs2477574
PubMed Link:
32703994
Variant Present in the following documents:
41598_2020_68649_MOESM2_ESM.xlsx, sheet 2
View BVdb publication page
Improving power in genetic-association studies via wavelet transformation.
Bmc Genetics
Jiang, Renfang R; Dong, Jianping J; Dai, Yilin Y
Publication Date: 2009-09-11
Variant appearance in text: rs2477574
PubMed Link:
19747393
Variant Present in the following documents:
Main text
1471-2156-10-53.pdf
View BVdb publication page
Analysis of multiple SNPs in a candidate gene or region.
Genetic Epidemiology
Chapman, Juliet J; Whittaker, John J
Publication Date: 2008-09
Variant appearance in text: rs2477574
PubMed Link:
18428428
Variant Present in the following documents:
Main text
View BVdb publication page
Improved power by use of a weighted score test for linkage disequilibrium mapping.
American Journal Of Human Genetics
Wang, Tao T; Elston, Robert C RC
Publication Date: 2007-02
Variant appearance in text: rs2477574
PubMed Link:
17236140
Variant Present in the following documents:
Main text
View BVdb publication page