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rs1126643

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1126643(C;T)
Make rs1126643(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position53051539
GeneITGA2
is asnp
is mentioned by
dbSNPrs1126643
dbSNP (old)rs1126643
ClinGenrs1126643
ebirs1126643
HLIrs1126643
Exacrs1126643
Gnomadrs1126643
Varsomers1126643
Maprs1126643
PheGenIrs1126643
Biobankrs1126643
1000 genomesrs1126643
hgdprs1126643
ensemblrs1126643
gopubmedrs1126643
geneviewrs1126643
scholarrs1126643
googlers1126643
pharmgkbrs1126643
gwascentralrs1126643
openSNPrs1126643
23andMers1126643
23andMe allrs1126643
SNP Nexus

SNPshotrs1126643
SNPdbers1126643
MSV3drs1126643
GWAS Ctlgrs1126643
GMAF0.3632
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 18830231OA-icon.png] prostate cancer rs3212649 (OR=1.67 (1.07-2.6), P=0.0009) and rs1126643 (OR=1.52 (1.01-2.28), P=0.0088).


[PMID 19786296] Platelet glycoprotein GP VI 13254C allele is an independent risk factor of premature myocardial infarction


[PMID 22133274OA-icon.png] Polymorphisms of PAI-1 and platelet GP Ia may associate with impairment of renal function and thrombocytopenia in Puumala hantavirus infection


[PMID 18936436OA-icon.png] Prevalence in the United States of selected candidate gene variants: Third National Health and Nutrition Examination Survey, 1991-1994.


[PMID 22015659] Mean platelet volume and integrin alleles correlate with levels of integrins alpha(IIb)beta(3) and alpha(2)beta(1) in acute coronary syndrome patients and normal subjects.


[PMID 24397542] Genetic polymorphism of ITGA2 C807T can increase the risk of Ischemic Stroke


[PMID 23533563OA-icon.png] Novel risk factors for premature peripheral arterial occlusive disease in non-diabetic patients: a case-control study.


[PMID 25901734] Effect of platelet receptor gene polymorphisms on outcomes in ST-elevation myocardial infarction patients after percutaneous coronary intervention


ClinVar
Risk rs1126643(T;T)
Alt rs1126643(T;T)
Reference Rs1126643(C;C)
Significance Non-pathogenic
Disease Platelet-type bleeding disorder 9
Variation info
Gene ITGA2
CLNDBN Platelet-type bleeding disorder 9
Reversed 0
HGVS NC_000005.9:g.52347369C>T
CLNSRC
CLNACC RCV000264523.1,



[PMID 28871283OA-icon.png] GPla Polymorphisms Are Associated with Outcomes in Patients at High Cardiovascular Risk.