Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1800629
rs1800629
TNF
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.030 GeneticVariation BEFREE These results indicate that higher level of serum TNF-α increases risk of CHD, while TNF-α rs1800629 A allele might contribute to higher risk for CHD due to the increase in TNF-α expression. 31324728

2019
dbSNP: rs1800629
rs1800629
TNF
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.030 GeneticVariation BEFREE Promoter variants of TNF-α rs1800629 and IL-10 rs1800871 are independently associated with the susceptibility of coronary artery disease in north Indian. 29734056

2018
dbSNP: rs1800629
rs1800629
TNF
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.030 GeneticVariation BEFREE The association of IFN-γ (+874 A/T; rs2430561), TNF-α (-308 G/A; rs1800629) and TNF-β (+252 A/G; rs909253) with Coronary Heart Disease (CHD) has not been rigorously tested in Indian population. 23159874

2013