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.




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