Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2074356
rs2074356
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03
Diabetes Mellitus, Non-Insulin-Dependent
0.810 1.000 1 2013 2016
dbSNP: rs11066280
rs11066280
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 3 2012 2013
dbSNP: rs2074356
rs2074356
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption
0.800 1.000 2 2011 2017
dbSNP: rs11066280
rs11066280
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.800 1.000 1 2010 2011
dbSNP: rs11066280
rs11066280
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03
CUI: C0013124
Disease: Drinking behavior processes
Drinking behavior processes
0.800 1.000 1 2013 2013
dbSNP: rs2074356
rs2074356
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03
CUI: C0005845
Disease: Blood urea nitrogen measurement
Blood urea nitrogen measurement
0.800 1.000 1 2012 2012
dbSNP: rs2074356
rs2074356
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.800 1.000 1 2010 2011
dbSNP: rs2074356
rs2074356
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio
0.800 1.000 1 2009 2009
dbSNP: rs2074356
rs2074356
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03
High density lipoprotein measurement
0.800 1.000 1 2011 2019
dbSNP: rs2074356
rs2074356
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 2 2012 2013
dbSNP: rs11066188
rs11066188
0.851 0.320 12 112172910 intron variant G/A;C snv 0.30; 4.1E-06
CUI: C0039685
Disease: Tetralogy of Fallot
Tetralogy of Fallot
0.700 1.000 1 2013 2013
dbSNP: rs11066188
rs11066188
0.851 0.320 12 112172910 intron variant G/A;C snv 0.30; 4.1E-06
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2009 2009
dbSNP: rs11066188
rs11066188
0.851 0.320 12 112172910 intron variant G/A;C snv 0.30; 4.1E-06
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs11066188
rs11066188
0.851 0.320 12 112172910 intron variant G/A;C snv 0.30; 4.1E-06
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism
0.700 1.000 1 2012 2012
dbSNP: rs11066280
rs11066280
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2011 2011
dbSNP: rs11066280
rs11066280
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2011 2011
dbSNP: rs11066280
rs11066280
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption
0.700 1.000 1 2013 2013
dbSNP: rs11066280
rs11066280
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder
0.700 1.000 1 2013 2013
dbSNP: rs11066280
rs11066280
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03
CUI: C0546837
Disease: Malignant neoplasm of esophagus
Malignant neoplasm of esophagus
0.700 1.000 1 2011 2011
dbSNP: rs2074356
rs2074356
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03
CUI: C0546837
Disease: Malignant neoplasm of esophagus
Malignant neoplasm of esophagus
0.700 1.000 1 2011 2011
dbSNP: rs2074356
rs2074356
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 1 2011 2011
dbSNP: rs2074356
rs2074356
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03
CUI: C0013124
Disease: Drinking behavior processes
Drinking behavior processes
0.700 1.000 1 2013 2013
dbSNP: rs2074356
rs2074356
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder
0.700 1.000 1 2013 2013
dbSNP: rs2074356
rs2074356
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03
Gamma glutamyl transferase measurement
0.700 1.000 1 2011 2011
dbSNP: rs2285809
rs2285809
1.000 0.120 12 112270622 intron variant T/C snv 0.16
Diabetes Mellitus, Insulin-Dependent
0.700 1.000 1 2008 2008