Variant ID: 9-132501881-A-C

NM_004878.4(PTGES):c.*9T>G

This variant was identified in 12 publications




Publications:


MicroRNA-binding site polymorphisms and risk of colorectal cancer: A systematic review and meta-analysis.

Cancer Medicine
M Gholami, B Larijani, F Sharifi, S Hasani-Ranjbar, R Taslimi, M Bastami, R Atlasi, MM Amoli
Publication Date: 2019-12

Variant appearance in text: rs2302821
PubMed Link: 31637880
Variant Present in the following documents:
  • Main text
View BVdb publication page



Multiphenotype association study of patients randomized to initiate antiretroviral regimens in AIDS Clinical Trials Group protocol A5202.

Pharmacogenetics And Genomics
A Verma, Y Bradford, SS Verma, SA Pendergrass, ES Daar, C Venuto, GD Morse, MD Ritchie, DW Haas
Publication Date: 2017-03

Variant appearance in text: rs2302821
PubMed Link: 28099408
Variant Present in the following documents:
  • Main text
View BVdb publication page



A Genetic Response Score for Hydrochlorothiazide Use: Insights From Genomics and Metabolomics Integration.

Hypertension (Dallas, Tex. : 1979)
MH Shahin, Y Gong, CW McDonough, DM Rotroff, AL Beitelshees, TJ Garrett, JG Gums, A Motsinger-Reif, AB Chapman, ST Turner, E Boerwinkle, RF Frye, O Fiehn, RM Cooper-DeHoff, R Kaddurah-Daouk, JA Johnson
Publication Date: 2016-09

Variant appearance in text: rs2302821
PubMed Link: 27381900
Variant Present in the following documents:
  • NIHMS793669-supplement-ONLINE_SUPPLEMENTARY.docx
View BVdb publication page



Impact of genetic polymorphisms on adenoma recurrence and toxicity in a COX2 inhibitor (celecoxib) trial: results from a pilot study.

Pharmacogenetics And Genomics
S Kraus, S Hummler, AT Toriola, EM Poole, D Scherer, J Kotzmann, KW Makar, D Kazanov, L Galazan, I Naumov, AE Coghill, D Duggan, B Gigic, N Arber, CM Ulrich
Publication Date: 2013-08

Variant appearance in text: rs2302821
PubMed Link: 23778325
Variant Present in the following documents:
  • Main text
  • NIHMS687149-supplement-Supplemental_material.doc
View BVdb publication page



Inherited variation at chromosome 12p13.33, including RAD52, influences the risk of squamous cell lung carcinoma.

Cancer Discovery
J Shi, N Chatterjee, M Rotunno, Y Wang, AC Pesatori, D Consonni, P Li, W Wheeler, P Broderick, M Henrion, T Eisen, Z Wang, W Chen, Q Dong, D Albanes, M Thun, MR Spitz, PA Bertazzi, NE Caporaso, SJ Chanock, CI Amos, RS Houlston, MT Landi
Publication Date: 2012-02

Variant appearance in text: rs2302821
PubMed Link: 22585858
Variant Present in the following documents:
  • NIHMS343818-supplement-1.pdf
View BVdb publication page



Associations between gene polymorphisms in fatty acid metabolism pathway and preterm delivery in a US urban black population.

Human Genetics
X Liu, G Wang, X Hong, HJ Tsai, R Liu, S Zhang, H Wang, C Pearson, K Ortiz, D Wang, E Hirsch, B Zuckerman, X Wang
Publication Date: 2012-03

Variant appearance in text: rs2302821
PubMed Link: 21847588
Variant Present in the following documents:
  • Main text
  • NIHMS714779-supplement-Supplemental.doc
View BVdb publication page



Variants of gene for microsomal prostaglandin E2 synthase show association with disease and severe inflammation in rheumatoid arthritis.

European Journal Of Human Genetics : Ejhg
M Korotkova, NA Daha, M Seddighzadeh, B Ding, AI Catrina, S Lindblad, TW Huizinga, RE Toes, L Alfredsson, L Klareskog, PJ Jakobsson, L Padyukov
Publication Date: 2011-08

Variant appearance in text: rs2302821
PubMed Link: 21448233
Variant Present in the following documents:
  • Main text
View BVdb publication page



Maternal and fetal genetic associations of PTGER3 and PON1 with preterm birth.

Plos One
KK Ryckman, NH Morken, MJ White, DR Velez, R Menon, SJ Fortunato, P Magnus, SM Williams, B Jacobsson
Publication Date: 2010-02-03

Variant appearance in text: rs2302821
PubMed Link: 20140262
Variant Present in the following documents:
  • pone.0009040.s003.doc
  • pone.0009040.s005.doc
View BVdb publication page



Genetic variation in prostaglandin E2 synthesis and signaling, prostaglandin dehydrogenase, and the risk of colorectal adenoma.

Cancer Epidemiology, Biomarkers & Prevention : A Publication Of The American Association For Cancer Research, Cosponsored By The American Society Of Preventive Oncology
EM Poole, L Hsu, L Xiao, RJ Kulmacz, CS Carlson, PS Rabinovitch, KW Makar, JD Potter, CM Ulrich
Publication Date: 2010-02

Variant appearance in text: rs2302821
PubMed Link: 20086108
Variant Present in the following documents:
  • NIHMS187592-supplement-Suppl_Tables_Figures.doc
View BVdb publication page



Common genetic variation in candidate genes and susceptibility to subtypes of breast cancer.

Cancer Epidemiology, Biomarkers & Prevention : A Publication Of The American Association For Cancer Research, Cosponsored By The American Society Of Preventive Oncology
N Mavaddat, AM Dunning, BA Ponder, DF Easton, PD Pharoah
Publication Date: 2009-01

Variant appearance in text: rs2302821
PubMed Link: 19124506
Variant Present in the following documents:
  • NIHMS3984-supplement-SuppTable1.doc
View BVdb publication page



Preterm birth in Caucasians is associated with coagulation and inflammation pathway gene variants.

Plos One
DR Velez, SJ Fortunato, P Thorsen, SJ Lombardi, SM Williams, R Menon
Publication Date: 2008-09-26

Variant appearance in text: rs2302821
PubMed Link: 18818748
Variant Present in the following documents:
  • pone.0003283.s001.doc
View BVdb publication page



Association between common variation in 120 candidate genes and breast cancer risk.

Plos Genetics
PD Pharoah, J Tyrer, AM Dunning, DF Easton, BA Ponder,
Publication Date: 2007-03-16

Variant appearance in text: rs2302821
PubMed Link: 17367212
Variant Present in the following documents:
  • pgen.0030042.st003.doc
View BVdb publication page



Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000340607.4 c.*9T>G - 3_prime_UTR_variant 3/3 -
ENST00000435588.2 n.22T>G - non_coding_transcript_exon_variant 1/2 -
ENST00000481476.1 n.597T>G - non_coding_transcript_exon_variant 4/4 -
NM_004878.5 c.*9T>G - 3_prime_UTR_variant 3/3 -