Variant: rs11066001 

    present in Gene: BRAP
    present in Chromosome: 12
    Position on Chromosome: 111681367
    Alleles of this Variant: T/C

rs11066001 in BRAP gene and Alcohol-Induced Disorders PMID 31591379 2019 Genome-wide association study of alcohol dependence in male Han Chinese and cross-ethnic polygenic risk score comparison.

rs11066001 in BRAP gene and Alcohol-Related Disorders PMID 31591379 2019 Genome-wide association study of alcohol dependence in male Han Chinese and cross-ethnic polygenic risk score comparison.

rs11066001 in BRAP gene and Alcoholic Intoxication, Chronic PMID 31591379 2019 Genome-wide association study of alcohol dependence in male Han Chinese and cross-ethnic polygenic risk score comparison.

rs11066001 in BRAP gene and Coronary heart disease PMID 21971053 2012 Genome-wide association study of coronary artery disease in the Japanese.

PMID 23364394 2013 A genome-wide association study of a coronary artery disease risk variant.

rs11066001 in BRAP gene and Malignant neoplasm of esophagus PMID 21642993 2011 Genome-wide association study identifies three new susceptibility loci for esophageal squamous-cell carcinoma in Chinese populations.