CCR3 c.116C>G ;(p.P39R)

Variant ID: 3-46306765-C-G

NM_178329.2(CCR3):c.116C>G;(p.P39R)

This variant was identified in 7 publications

View GRCh38 version.




Publications:


Convergent transcriptomic and genomic evidence supporting a dysregulation of CXCL16 and CCL5 in Alzheimer's disease.

Alzheimer'S Research & Therapy
Li, Xiao X; Zhang, Deng-Feng DF; Bi, Rui R; Tan, Li-Wen LW; Chen, Xiaogang X; Xu, Min M; Yao, Yong-Gang YG
Publication Date: 2023-01-21

Variant appearance in text: rs5742906
PubMed Link: 36670424
Variant Present in the following documents:
  • 13195_2022_1159_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page



Some Common SNPs of the T-Cell Homeostasis-Related Genes Are Associated with Multiple Sclerosis, but Not with the Clinical Manifestations of the Disease, in the Polish Population.

Journal Of Immunology Research
Chorąży, Monika M; Wawrusiewicz-Kurylonek, Natalia N; Adamska-Patruno, Edyta E; Zajkowska, Olga O; Kapica-Topczewska, Katarzyna K; Posmyk, Renata R; Krętowski, Adam Jacek AJ; Kochanowicz, Jan J; Kułakowska, Alina A
Publication Date: 2020

Variant appearance in text: rs5742906
PubMed Link: 33224992
Variant Present in the following documents:
  • Main text
  • JIR2020-8838014.pdf
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XomAnnotate: Analysis of Heterogeneous and Complex Exome- A Step towards Translational Medicine.

Plos One
Talukder, Asoke K AK; Ravishankar, Shashidhar S; Sasmal, Krittika K; Gandham, Santhosh S; Prabhukumar, Jyothsna J; Achutharao, Prahalad H PH; Barh, Debmalya D; Blasi, Francesco F
Publication Date: 2015

Variant appearance in text: rs5742906
PubMed Link: 25905921
Variant Present in the following documents:
  • pone.0123569.s008.xls, sheet 1
View BVdb publication page



A candidate gene association study of 77 polymorphisms in migraine.

The Journal Of Pain
Schürks, Markus M; Kurth, Tobias T; Buring, Julie E JE; Zee, Robert Y L RY
Publication Date: 2009-07

Variant appearance in text: rs5742906
PubMed Link: 19559392
Variant Present in the following documents:
  • Main text
View BVdb publication page



Association of 77 polymorphisms in 52 candidate genes with blood pressure progression and incident hypertension: the Women's Genome Health Study.

Journal Of Hypertension
Conen, David D; Cheng, Suzanne S; Steiner, Lori L LL; Buring, Julie E JE; Ridker, Paul M PM; Zee, Robert Y L RY
Publication Date: 2009-03

Variant appearance in text: rs5742906
PubMed Link: 19330901
Variant Present in the following documents:
  • Main text
View BVdb publication page



A meta-analysis of candidate gene polymorphisms and ischemic stroke in 6 study populations: association of lymphotoxin-alpha in nonhypertensive patients.

Stroke
Wang, Xingyu X; Cheng, Suzanne S; Brophy, Victoria H VH; Erlich, Henry A HA; Mannhalter, Christine C; Berger, Klaus K; Lalouschek, Wolfgang W; Browner, Warren S WS; Shi, Yu Y; Ringelstein, E Bernd EB; Kessler, Christof C; Luedemann, Jan J; Lindpaintner, Klaus K; Liu, Lisheng L; Ridker, Paul M PM; Zee, Robert Y L RY; Cook, Nancy R NR; ,
Publication Date: 2009-03

Variant appearance in text: rs5742906
PubMed Link: 19131662
Variant Present in the following documents:
  • Main text
View BVdb publication page



The chemokine (C-C-motif) receptor 3 (CCR3) gene is linked and associated with age at menarche in Caucasian females.

Human Genetics
Yang, Fang F; Xiong, Dong-hai DH; Guo, Yan Y; Shen, Hui H; Xiao, Peng P; Zhang, Feng F; Jiang, Hui H; Recker, Robert R RR; Deng, Hong-wen HW
Publication Date: 2007-03

Variant appearance in text: rs5742906
PubMed Link: 17146638
Variant Present in the following documents:
  • Main text
View BVdb publication page