SNP information rs657152

Research and publications:

  18514160   Phosphodiesterase 8B gene variants are associated with serum TSH levels and thyroid function.

  18604267   Novel association of ABO histo-blood group antigen with soluble ICAM-1: results of a genome-wide association study of 6,578 women.

  18940312   Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes

  19474294   Potential etiologic and functional implications of genome-wide association loci for human diseases and traits

  19648918   Genome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancer.

  19729612   Genome-wide association identifies the ABO blood group as a major locus associated with serum levels of soluble E-selectin.

  20103627   Pancreatic cancer risk and ABO blood group alleles: results from the pancreatic cancer cohort consortium.

  20147318   Genetic variants in ABO blood group region, plasma soluble E-selectin levels and risk of type 2 diabetes.

  20529992   Genetic regulation of serum phytosterol levels and risk of coronary artery disease.

  20648472   PNPLA3 variants specifically confer increased risk for histologic nonalcoholic fatty liver disease but not metabolic disease

  20833654   Mapping of numerous disease-associated expression polymorphisms in primary peripheral blood CD4+ lymphocytes.

  21084706   Genetic regulation of platelet receptor expression and function: application in clinical practice and drug development.

  21239051   Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studies.

  21463476   Genetic variation within the anticoagulant, procoagulant, fibrinolytic and innate immunity pathways as risk factors for venous thromboembolism.

  21534939   Genetic variants associated with Von Willebrand factor levels in healthy men and women identified using the HumanCVD BeadChip.

  21829393   Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases.

  21980494   Genetics of venous thrombosis: insights from a new genome wide association study.

  22025780   FUT2 nonsecretor status links type 1 diabetes susceptibility and resistance to infection.

  22125638   Pancreatic cancer susceptibility loci and their role in survival.

  22291609   A genome-wide association scan on the levels of markers of inflammation in Sardinians reveals associations that underpin its complex regulation.

  22523087   Pathway analysis of genome-wide association study data highlights pancreatic development genes as susceptibility factors for pancreatic cancer.

  23133757   ABO Blood Groups and Cardiovascular Diseases.

  23152778   Establishment and characterization of a highly tumourigenic and cancer stem cell enriched pancreatic cancer cell line as a well defined model system.

  23251661   Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population

  23408906   A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.

  23707316   High intestinal cholesterol absorption is associated with cardiovascular disease and risk alleles in ABCG8 and ABO: evidence from the LURIC and YFS cohorts and from a meta-analysis.

  23816557   Re-evaluation of ABO gene polymorphisms detected in a genome-wide association study and risk of pancreatic ductal adenocarcinoma in a Chinese population.

  24586218   Pleiotropic effect of common variants at ABO Glycosyltranferase locus in 9q32 on plasma levels of pancreatic lipase and angiotensin converting enzyme.

  25025429   Single nucleotide polymorphisms with cis-regulatory effects on long non-coding transcripts in human primary monocytes.

  25436638   Genetic variants associated with serum thyroid stimulating hormone (TSH) levels in European Americans and African Americans from the eMERGE Network.

  26105150   Rare and low-frequency variants and their association with plasma levels of fibrinogen, FVII, FVIII, and vWF.

  26111702   Pancreatic cancer-associated gene polymorphisms in a nation-wide cohort of p16-Leiden germline mutation carriers; a case-control study.

  26286125   Coagulation factor XII genetic variation, ex vivo thrombin generation, and stroke risk in the elderly: results from the Cardiovascular Health Study.

  26888256   Novel genetic predictors of venous thromboembolism risk in African Americans.

  28686695   Coronary artery disease-associated genetic variants and biomarkers of inflammation.

  29048744   Comorbidity of Alcohol Use Disorder and Chronic Pain: Genetic Influences on Brain Reward and Stress Systems.

  32093636   Association of ABO polymorphisms and pancreatic Cancer/ Cardiocerebrovascular disease: a meta-analysis.

  32558485   Genomewide Association Study of Severe Covid-19 with Respiratory Failure.

  32899439   Genetic Hypothesis and Pharmacogenetics Side of Renin-Angiotensin-System in COVID-19.

  33894687   ABO blood groups, COVID-19 infection and mortality.

  34483600   SNP rs657152 Is Not Associated with the Level of Viral Load in COVID-19 or the Probability of Disease in the Population of Caucasians in Eastern Siberia.

  34764675   Variation of Genomic Sites Associated with Severe Covid-19 Across Populations: Global and National Patterns.

  35196333   Evaluation of the genetic risk for COVID-19 outcomes in COPD and differences among worldwide populations.

  35212764   Proteomic profiling identifies novel proteins for genetic risk of severe COVID-19: the Atherosclerosis Risk in Communities Study.