rs2383206, CDKN2B-AS1

N. diseases: 17
Disease: Coronary heart disease ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
0.720 GeneticVariation GWASDB A genome-wide association study of a coronary artery disease risk variant. 23364394 2013
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
0.720 GeneticVariation BEFREE With the exception of rs1333040, whites with at least one copy of the 9p21 SNP risk alleles were found to have CHD from 1.45 (rs10116277) to 4.77 (rs2383206) years earlier than those with the wild-type alleles. 21375403 2011
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
0.720 GeneticVariation BEFREE Using the combined TDT/S-TDT test, the 3 single nucleotide polymorphisms (SNP), rs10757274, rs2383206 and rs1333049, were strongly associated with early-onset CHD (p = 2.7 x 10(-6), 2.7 x 10(-6), 3.8 x 10(-7), respectively). 18957718 2008