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:
Research and publications:
18987759 Genetic testing for atherosclerosis risk: inevitability or pipe dream?
19578366 Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility.
23587006 Validation of reported genetic risk factors for periodontitis in a large-scale replication study.
26483964 Genomic Study of Cardiovascular Continuum Comorbidity.
28580310 ANRIL Genetic Variants in Iranian Breast Cancer Patients.
29713948 Association Study of ANRIL Genetic Variants and Multiple Sclerosis.
29802154 Association between long non-coding RNA polymorphisms and cancer risk: a meta-analysis.
31773399 ANRIL Variants Are Associated with Risk of Neuropsychiatric Conditions.
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.
34615528 Genetic and epigenetic associations of ANRIL with coronary artery disease and risk factors.
35866908 ANRIL polymorphisms in psoriasis vulgaris patients in northern China.