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SNP information rs11066280

RS11066280

Normal allele: TT

Polymorphism rs11066280 is related to topics like this:

Heart attack genetic

Genetic predisposition, also referred to as familial predisposition, is a crucial risk factor for...

Heart disease genetic

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


Research and publications:

  21367945   Genome-wide association studies of alcohol intake--a promising cocktail?

  21572416   Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians.

  22507220   Epidemiologic differences in esophageal cancer between Asian and Western populations.

  22865593   Distinct genetic association at the PLCE1 locus with oesophageal squamous cell carcinoma in the South African population.

  23364009   Common variants at 12q24 are associated with drinking behavior in Han Chinese.

  23629646   Epidemiology of esophageal cancer in Japan and China.

  24142389   Male-specific genetic effect on hypertension and metabolic disorders.

  25133033   Epidemiological studies of esophageal cancer in the era of genome-wide association studies.

  25464127   On the analysis of a repeated measure design in genome-wide association analysis.

  26675016   A Genome-Wide Association Study Uncovers a Genetic Locus Associated with Thoracic-to-Hip Ratio in Koreans.

  26770579   Genetic variants at 6p21, 10q23, 16q21 and 22q12 are associated with esophageal cancer risk in a Chinese Han population.

  26891264   No Interaction with Alcohol Consumption, but Independent Effect of C12orf51 (HECTD4) on Type 2 Diabetes Mellitus in Korean Adults Aged 40-69 Years: The KoGES_Ansan and Ansung Study.

  27181629   Identification of rs671, a common variant of ALDH2, as a gout susceptibility locus.

  27437086   Allele Frequencies of the Single Nucleotide Polymorphisms Related to the Body Burden of Heavy Metals in the Korean Population and Their Ethnic Differences.

  28212632   Exome-wide association study identifies genetic polymorphisms of C12orf51, MYL2, and ALDH2 associated with blood lead levels in the general Korean population.

  28424424   Leukocyte telomere length-related genetic variants in ACYP2 contribute to the risk of esophageal carcinoma in Chinese Han population.

  28562329   Identification of polymorphisms in 12q24.1, ACAD10, and BRAP as novel genetic determinants of blood pressure in Japanese by exome-wide association studies.

  29930802   Identification of four genes as novel susceptibility loci for early-onset type 2 diabetes mellitus, metabolic syndrome, or hyperuricemia.

  29942042   A decade in psychiatric GWAS research.

  35205218   Variation in Genotype and DNA Methylation Patterns Based on Alcohol Use and CVD in the Korean Genome and Epidemiology Study (KoGES).

  35713687   The potential effects of HECTD4 variants on fasting glucose and triglyceride levels in relation to prevalence of type 2 diabetes based on alcohol intake.

CGRP migraine

Migraine affects a significant portion of the adult population in most countries, with a higher...

Factor 5 blood clotting disorder

Thrombophilia, an increased tendency to form abnormal blood clots that can obstruct blood vessels,...

Memory genes

Despite being often overlooked, the brain possesses an impressive ability to restrict the creation...

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