rs1878406, None

N. diseases: 7
Disease: Atherosclerosis ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
0.810 GeneticVariation BEFREE Our results do not confirm association between ABO rs579459, PPAP2B rs17114036, ADAMTS7 rs3825807, PIK3CG rs17398575, and EDNRA rs1878406 and subclinical atherosclerosis and CV disease in RA. 24795506 2014
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
0.810 GeneticVariation GWASDB Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque. 21909108 2011
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
0.810 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque. 21909108 2011