Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs7442201
rs7442201
Entrez Id: 27065
Gene Symbol: NSG1
NSG1
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent 		0.700 GeneticVariation GWASCAT Genome-wide association study of coronary artery calcified atherosclerotic plaque in African Americans with type 2 diabetes. 29221444 2017
dbSNP: rs7442201
rs7442201
Entrez Id: 27065
Gene Symbol: NSG1
NSG1
CUI: C1611184
Disease:
Calcification of coronary artery 		0.700 GeneticVariation GWASCAT Genome-wide association study of coronary artery calcified atherosclerotic plaque in African Americans with type 2 diabetes. 29221444 2017
dbSNP: rs3792686
rs3792686
Entrez Id: 27065
Gene Symbol: NSG1
NSG1
CUI: C0001973
Disease:
Alcoholic Intoxication, Chronic 		0.700 GeneticVariation GWASDB A novel, functional and replicable risk gene region for alcohol dependence identified by genome-wide association study. 22096494 2011
dbSNP: rs2044
rs2044
Entrez Id: 27065;53407
Gene Symbol: NSG1;STX18
NSG1;STX18
CUI: C0010068
Disease:
Coronary heart disease 		0.010 GeneticVariation BEFREE Analysis of associations of these genetic variations with the risk of CHD showed that rs12644497 (P value=0.017<0.05) was associated with the risk of CHD, specifically VSD and ASD, whereas rs12504020 (P value=0.560>0.05) and rs2044 (P value=0.972>0.05) were not. 27816473 2017