Normal allele: CC
Polymorphism rs657152 is related to topics like this:
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.