SNP information rs1048990

Research and publications:

  16845397   A functional SNP in PSMA6 confers risk of myocardial infarction in the Japanese population.

  17767904   Genetic and genomic insights into the molecular basis of atherosclerosis.

  18231128   The exon 1-8C/G SNP in the PSMA6 gene contributes only a small amount to the burden of myocardial infarction in 6946 cases and 2720 controls from a United Kingdom population.

  19272601   The functional variant rs1048990 in PSMA6 is associated with susceptibility to myocardial infarction in a Chinese population.

  19282875   Replication studies for the association of PSMA6 polymorphism with coronary artery disease in East Asian populations.

  19503741   Coding variant Met72Thr in the PEDF gene and risk of neovascular age-related macular degeneration and polypoidal choroidal vasculopathy.

  19624571   Haplotypes encompassing the KIAA0391 and PSMA6 gene cluster confer a genetic link for myocardial infarction and coronary artery disease.

  19753309   SOD2 gene polymorphisms in neovascular age-related macular degeneration and polypoidal choroidal vasculopathy.

  20157514   Positive association of common variants in CD36 with neovascular age-related macular degeneration.

  20817676   Human single-nucleotide polymorphisms alter p53 sequence-specific binding at gene regulatory elements.

  22310064   Polymorphisms of LTA, LGALS2, and PSMA6 genes and coronary atherosclerosis: a pathological study of 1503 consecutive autopsy cases.

  22882272   Genetic variants associated with myocardial infarction in the PSMA6 gene and Chr9p21 are also associated with ischaemic stroke.

  23111455   Quantitative assessment of the influence of PSMA6 variant (rs1048990) on coronary artery disease risk.

  24205329   Detection of regulatory SNPs in human genome using ChIP-seq ENCODE data.

  24455213   Association of obesity with proteasomal gene polymorphisms in children.

  24490108   Genetics of proteasome diseases.

  24875235   Juvenile idiopathic arthritis subtype- and sex-specific associations with genetic variants in the PSMA6/PSMC6/PSMA3 gene cluster.

  25375907   Evaluation of proteasomal gene polymorphisms in Lithuanian patients with asthma.

  25606411   PSMA6 (rs2277460, rs1048990), PSMC6 (rs2295826, rs2295827) and PSMA3 (rs2348071) genetic diversity in Latvians, Lithuanians and Taiwanese.

  26661414   Genetic variations in the PSMA3, PSMA6 and PSMC6 genes are associated with type 1 diabetes in Latvians and with expression level of number of UPS-related and T1DM-susceptible genes in HapMap individuals.

  27766139   Methodology for single nucleotide polymorphism selection in promoter regions for clinical use. An example of its applicability.

  30182779   Genetic susceptibility to cerebrovascular disease: A systematic review.

  32582717   The Role of Transcription Factor 21 in Epicardial Cell Differentiation and the Development of Coronary Heart Disease.

  33466296   Discovering Genotype Variants in an Infant with VACTERL through Clinical Exome Sequencing: A Support for Personalized Risk Assessment and Disease Prevention.

  33683357   Evaluating human autosomal loci for sexually antagonistic viability selection in two large biobanks.

  33767773   Genetic variations in the PSMA6 and PSMC6 proteasome genes are associated with multiple sclerosis and response to interferon-β therapy in Latvians.

  33996179   Polymorphism of Proteasomal Genes Can Be a Risk Factor for Systemic Autoimmune Diseases in Children.

  34575036   The Genetic Variants of NOTCH3 (6746T>C) and PSMA6 (-8C>G) as Possible Risk Factors of Psoriasis Development.