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SNP information rs1333048

RS1333048

Normal allele: AA

ANRIL genetic variation is strongly associated with the risk of myocardial infarction and coronary heart disease.

Polymorphism rs1333048 is related to topics like this:

Heart disease genetic

Although genetics can be a major factor in the development of certain heart diseases, individuals...


Research and publications:

  18987759   Genetic testing for atherosclerosis risk: inevitability or pipe dream?

  19214202   Identification of a shared genetic susceptibility locus for coronary heart disease and periodontitis.

  19578366   Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility.

  20696043   Replication of the association of chromosomal region 9p21.3 with generalized aggressive periodontitis (gAgP) using an independent case-control cohort.

  20858905   Association of single nucleotide polymorphisms on chromosome 9p21.3 with platelet reactivity: a potential mechanism for increased vascular disease.

  23587006   Validation of reported genetic risk factors for periodontitis in a large-scale replication study.

  26348353   A Lead ANRIL Polymorphism Is Associated with Elevated CRP Levels in Periodontitis: A Pilot Case-Control Study.

  26483964   Genomic Study of Cardiovascular Continuum Comorbidity.

  26958643   Detailed analysis of association between common single nucleotide polymorphisms and subclinical atherosclerosis: The Multi-ethnic Study of Atherosclerosis.

  26999117   Intronic Polymorphisms in the CDKN2B-AS1 Gene Are Strongly Associated with the Risk of Myocardial Infarction and Coronary Artery Disease in the Saudi Population.

  27168739   Association of single nucleotide polymorphism rs2076185 in chromosome 6P24.1 with premature coronary artery diseases in Chinese Han population.

  27509131   A Putative Association of a Single Nucleotide Polymorphism in GPR126 with Aggressive Periodontitis in a Japanese Population.

  28580310   ANRIL Genetic Variants in Iranian Breast Cancer Patients.

  28621612   Association of ANRIL gene polymorphisms with prostate cancer and benign prostatic hyperplasia in an Iranian population.

  29713948   Association Study of ANRIL Genetic Variants and Multiple Sclerosis.

  29802154   Association between long non-coding RNA polymorphisms and cancer risk: a meta-analysis.

  30030838   Validation of reported GLT6D1 (rs1537415), IL10 (rs6667202), and ANRIL (rs1333048) single nucleotide polymorphisms for aggressive periodontitis in a Brazilian population.

  30364300   Interaction between a variant of chromosome 9p21.3 locus and diet antioxidant capacity on metabolic syndrome in Tehrani adults.

  30600348   Dietary patterns interact with chromosome 9p21 rs1333048 polymorphism on the risk of obesity and cardiovascular risk factors in apparently healthy Tehrani adults.

  31773399   ANRIL Variants Are Associated with Risk of Neuropsychiatric Conditions.

  31812071   Genetic variants within ANRIL (antisense non coding RNA in the INK4 locus) are associated with risk of psoriasis.

  32152937   Application of Artificial Neural Network for Prediction of Risk of Multiple Sclerosis Based on Single Nucleotide Polymorphism Genotypes.

  32248921   9p21.3 coronary artery disease risk locus and interferon alpha 21: Association study in an Asian Indian population.

  32623644   Association Analysis of ANRIL Polymorphisms and Haplotypes with Autism Spectrum Disorders.

  33170163   Study of a supplement and a genetic test for lymphedema management.

  33186076   Long non-coding RNA ANRIL polymorphisms in papillary thyroid cancer and its severity.

  34036557   Discrimination of Patients with Prostate Cancer from Healthy Persons Using a Set of Single Nucleotide Polymorphisms.

  34615528   Genetic and epigenetic associations of ANRIL with coronary artery disease and risk factors.

  35866908   ANRIL polymorphisms in psoriasis vulgaris patients in northern China.

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