IL6R c.458+1298C>G

Variant ID: 1-154404380-C-G

NM_000565.3(IL6R):c.458+1298C>G

This variant was identified in 8 publications

View GRCh38 version.




Publications:


Circulating S100A4 as a prognostic biomarker for patients with nonparoxysmal atrial fibrillation after catheter ablation.

Annals Of Translational Medicine
Qian, Lijun L; Gong, Jinlong J; Ma, Wenjie W; Sun, Yan Y; Hong, Jian J; Xu, Di D; Chu, Ming M
Publication Date: 2021-09

Variant appearance in text: rs7549338
PubMed Link: 34733952
Variant Present in the following documents:
  • Main text
  • atm-09-18-1400.pdf
View BVdb publication page



Genome-wide association study of high-sensitivity C-reactive protein, D-dimer, and interleukin-6 levels in multiethnic HIV+ cohorts.

Aids (London, England)
Sherman, Brad T BT; Hu, Xiaojun X; Singh, Kanal K; Haine, Lillian L; Rupert, Adam W AW; Neaton, James D JD; Lundgren, Jens D JD; Imamichi, Tomozumi T; Chang, Weizhong W; Lane, H Clifford HC; ,
Publication Date: 2021-02-02

Variant appearance in text: rs7549338
PubMed Link: 33095540
Variant Present in the following documents:
  • aids-35-193-s003.xlsx, sheet 1
View BVdb publication page



Sex-Specific Genetic Susceptibility to Adverse Neurodevelopmental Outcome in Offspring of Pregnancies at Risk of Early Preterm Delivery.

American Journal Of Perinatology
Varner, Michael W MW; Costantine, Maged M MM; Jablonski, Kathleen A KA; Rouse, Dwight J DJ; Mercer, Brian M BM; Leveno, Kenneth J KJ; Reddy, Uma M UM; Buhimschi, Catalin C; Wapner, Ronald J RJ; Sorokin, Yoram Y; Thorp, John M JM; Ramin, Susan M SM; Malone, Fergal D FD; Carpenter, Marshall M; O'sullivan, Mary J MJ; Peaceman, Alan M AM; Dudley, Donald J DJ; Caritis, Steve N SN; ,
Publication Date: 2020-02

Variant appearance in text: rs7549338
PubMed Link: 30731481
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic Variation, Magnesium Sulfate Exposure, and Adverse Neurodevelopmental Outcomes Following Preterm Birth.

American Journal Of Perinatology
Clark, Erin A S EAS; Weiner, Steven J SJ; Rouse, Dwight J DJ; Mercer, Brian M BM; Reddy, Uma M UM; Iams, Jay D JD; Wapner, Ronald J RJ; Sorokin, Yoram Y; Malone, Fergal D FD; O'Sullivan, Mary J MJ; Peaceman, Alan M AM; Hankins, Gary D V GDV; Dudley, Donald J DJ; Caritis, Steve N SN; ,
Publication Date: 2018-08

Variant appearance in text: rs7549338
PubMed Link: 29510423
Variant Present in the following documents:
  • Main text
View BVdb publication page



Proficiency of data interpretation: identification of signaling SNPs/specific loci for coronary artery disease.

Database : The Journal Of Biological Databases And Curation
Cheema, Asma N AN; Rosenthal, Samantha L SL; Ilyas Kamboh, M M
Publication Date: 2017-01-01

Variant appearance in text: rs7549338
PubMed Link: 29220472
Variant Present in the following documents:
  • Main text
  • bax078.pdf
View BVdb publication page



Lipid-induced epigenomic changes in human macrophages identify a coronary artery disease-associated variant that regulates PPAP2B Expression through Altered C/EBP-beta binding.

Plos Genetics
Reschen, Michael E ME; Gaulton, Kyle J KJ; Lin, Da D; Soilleux, Elizabeth J EJ; Morris, Andrew J AJ; Smyth, Susan S SS; O'Callaghan, Christopher A CA
Publication Date: 2015-04

Variant appearance in text: rs7549338
PubMed Link: 25835000
Variant Present in the following documents:
  • Main text
  • pgen.1005061.pdf
View BVdb publication page



Genome-wide association study of CSF levels of 59 alzheimer's disease candidate proteins: significant associations with proteins involved in amyloid processing and inflammation.

Plos Genetics
Kauwe, John S K JS; Bailey, Matthew H MH; Ridge, Perry G PG; Perry, Rachel R; Wadsworth, Mark E ME; Hoyt, Kaitlyn L KL; Staley, Lyndsay A LA; Karch, Celeste M CM; Harari, Oscar O; Cruchaga, Carlos C; Ainscough, Benjamin J BJ; Bales, Kelly K; Pickering, Eve H EH; Bertelsen, Sarah S; , ; Fagan, Anne M AM; Holtzman, David M DM; Morris, John C JC; Goate, Alison M AM
Publication Date: 2014-10

Variant appearance in text: rs7549338
PubMed Link: 25340798
Variant Present in the following documents:
  • pgen.1004758.s006.xlsx, sheet 1
View BVdb publication page



Genetic contributions to disparities in preterm birth.

Pediatric Research
Anum, Emmanuel A EA; Springel, Edward H EH; Shriver, Mark D MD; Strauss, Jerome F JF
Publication Date: 2009-01

Variant appearance in text: rs7549338
PubMed Link: 18787421
Variant Present in the following documents:
  • Main text
View BVdb publication page