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SNP rs5918
Basic Information
Name
rs5918
Chromosome
17
Position
47283364
Weight of evidence
58
Genotype Frequency
Allele Frequency
Additional Information
SNPedia (4)
PLoS (8)
Mendeley (22)
Personal Genome Project (0)
Genome.gov (0)
Other users (1707)
Comments (0)
Links to SNPedia
Title
Summary
rs5918 T/T
Average
rs5918 C/C
Mi risk, aspirin resistance
rs5918 C/T
Mi risk, aspirin resistance
rs5918 A/A
No summary provided.
Note: For some SNPs, testing providers detect the genotype from the opposite strand of DNA, so that the genotypes listed on openSNP don't appear here. In those cases, please replace "A" by "T" or "G" by "C" (and vice-versa).
Publications on this SNP on the Public Library of Science:
First Author
Title
Year of Publication
# of readers
Annie M. Bérard
Novel Risk Factors for Premature Peripheral Arterial Occlusive Disease in Non-Diabetic Patients: A Case-Control Study
2013
4279
Charles Kooperberg
Can Biomarkers Identify Women at Increased Stroke Risk? The Women's Health Initiative Hormone Trials
2007
9196
Christopher N. Floyd
The PlA1/A2 Polymorphism of Glycoprotein IIIa as a Risk Factor for Stroke: A Systematic Review and Meta-Analysis
2014
2330
Yan Zhang
Genetic Variation of ITGB3 Is Associated with Asthma in Chinese Han Children
2013
2606
Morten Würtz
Genetic Determinants of On-Aspirin Platelet Reactivity: Focus on the Influence of
PEAR1
2014
3237
Xunsha Sun
The -7351C/T Polymorphism in the TPA Gene and Ischemic Stroke Risk: A Meta-Analysis
2013
2961
Tonia C. Rothuizen
Candidate Gene Analysis of Mortality in Dialysis Patients
2015
1645
Marisa L. R. Cunha
Whole exome sequencing in thrombophilic pedigrees to identify genetic risk factors for venous thromboembolism
2017
1525
Publications on this SNP on Mendeley
First Author
Title
Pub. Year
# of Readers
DOI
G. Allen Burton
Sediment toxicology evaluations, their niche in ecological assessments
1992
5
10.1016/j.jstrokecerebrovasdis.2009.10.011
M Neri
Impact of COX-2 rs5275 and rs20417 and GPIIIa rs5918 polymorphisms on 90-day ischemic stroke functional outcome: a novel finding
2010
1
-
F Ballesteros
Idiopathic sudden sensorineural hearing loss: classic cardiovascular and new genetic risk factors
2012
1
P Stafford
Immunologic and structural analysis of eight novel domain-deletion beta3 integrin peptides designed for detection of HPA-1 antibodies.
2008
3
-
G Altarescu
Preimplantation genetic diagnosis for fetal neonatal alloimmune thrombocytopenia due to antihuman platelet antigen maternal antibodies
2012
1
-
Joshua W. Knowles
Association of polymorphisms in platelet and hemostasis system genes with acute myocardial infarction
2007
4
10.1016/j.ahj.2007.05.021
T. Eldar Geva
Preimplantation Genetic Diagnosis for Fetal Neonatal Alloimmune Thrombocytopenia Due to Antihuman Platelet Antigen Maternal Antibodies
2012
2
10.1097/AOG.0b013e318242a11d
Anna Jakubowska
The Leu33Pro polymorphism in the ITGB3 gene does not modify BRCA1/2-associated breast or ovarian cancer risks: results from a multicenter study among 15,542 BRCA1 and BRCA2 mutation carriers.
2010
2
10.1007/s10549-009-0595-7
A M Kucharska-Newton
Association of the platelet GPIIb/IIIa polymorphism with atherosclerotic plaque morphology: the Atherosclerosis Risk in Communities (ARIC) Study
2011
3
10.1016/j.atherosclerosis.2011.01.038
Pekka Karhunen
Polymorphisms of PAI-1 and platelet GP Ia may associate with impairment of renal function and thrombocytopenia in Puumala hantavirus infection
2012
3
10.1016/j.thromres.2011.11.007
Man-Huei Chang
Genetic variants associated with fasting blood lipids in the U.S. population: Third National Health and Nutrition Examination Survey.
2010
2
10.1186/1471-2350-11-62
Anna M. Kucharska-Newton
Association of the platelet GPIIb/IIIa polymorphism with atherosclerotic plaque morphology: The Atherosclerosis Risk in Communities (ARIC) Study
2011
8
10.1016/j.atherosclerosis.2011.01.038
M H Chang
Genetic variants associated with fasting blood lipids in the U.S. population: Third National Health and Nutrition Examination Survey
2010
2
10.1186/1471-2350-11-62
Joshua W Knowles
Association of polymorphisms in platelet and hemostasis system genes with acute myocardial infarction.
2007
1
-
S Schmidt
Association of the platelet GPIIb/IIIa polymorphism with atherosclerotic plaque morphology: the Atherosclerosis Risk in Communities (ARIC) Study
2011
1
-
Joshua W Knowles
Association of polymorphisms in platelet and hemostasis system genes with acute myocardial infarction.
2007
4
10.1016/j.ahj.2007.05.021
K E Payne
Immunologic and structural analysis of eight novel domain-deletion beta3 integrin peptides designed for detection of HPA-1 antibodies
2008
1
-
Asem Surindro Singh
Genetic association and gene-gene interaction analyses suggest likely involvement of ITGB3 and TPH2 with autism spectrum disorder (ASD) in the Indian population.
2013
1
10.1016/j.pnpbp.2013.04.015
Man-huei Chang
Genetic variants associated with fasting blood lipids in the U.S. population: Third National Health and Nutrition Examination Survey.
2010
6
10.1186/1471-2350-11-62
Anna Jakubowska
The Leu33Pro polymorphism in the ITGB3 gene does not modify BRCA1/2-associated breast or ovarian cancer risks: results from a multicenter study among 15,542 BRCA1 and BRCA2 mutation carriers.
2010
3
10.1007/s10549-009-0595-7
Zuzana Motovska
Platelet glycoprotein GP VI 13254C allele is an independent risk factor of premature myocardial infarction.
2010
2
10.1016/j.thromres.2009.09.002
P Stafford
Immunologic and structural analysis of eight novel domain-deletion beta3 integrin peptides designed for detection of HPA-1 antibodies.
2008
4
10.1111/j.1538-7836.2007.02858.x
Evidence compiled by the
Personal Genome Project
There are no results from the
Personal Genome Project
yet. Please come back later.
Publications listed by
Genome.gov
There are no results from
genome.gov
yet. Please come back later.
Users who share this SNP:
Genome Browser