Source: GWASCAT

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: rs11066280
rs11066280
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 3 2011 2015
dbSNP: rs11066280
rs11066280
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
0.700 1.000 3 2011 2015
dbSNP: rs11066280
rs11066280
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03
Alanine aminotransferase measurement
0.700 1.000 2 2011 2019
dbSNP: rs11066280
rs11066280
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03
Serum Alanine Aminotransferase Measurement
0.700 1.000 2 2011 2019
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 2 2011 2019
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: rs1005902
rs1005902
12 112229871 missense variant T/C;G snv 4.1E-06; 0.42
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure
0.700 1.000 1 2016 2016
dbSNP: rs11066188
rs11066188
0.851 0.320 12 112172910 intron variant G/A;C snv 0.30; 4.1E-06
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
0.700 1.000 1 2016 2016
dbSNP: rs11066188
rs11066188
0.851 0.320 12 112172910 intron variant G/A;C snv 0.30; 4.1E-06
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.700 1.000 1 2016 2016
dbSNP: rs11066188
rs11066188
0.851 0.320 12 112172910 intron variant G/A;C snv 0.30; 4.1E-06
CUI: C0007570
Disease: Celiac Disease
Celiac Disease
0.700 1.000 1 2016 2016
dbSNP: rs11066194
rs11066194
1.000 0.040 12 112212323 intron variant A/G snv 4.8E-02
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.700 1.000 1 2018 2018
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 1 2012 2013
dbSNP: rs11066280
rs11066280
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure)
0.700 1.000 1 2018 2018
dbSNP: rs11066280
rs11066280
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03
Aspartate aminotransferase measurement
0.700 1.000 1 2019 2019
dbSNP: rs11066280
rs11066280
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.710 1.000 1 2014 2015
dbSNP: rs11066280
rs11066280
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2016 2016
dbSNP: rs11066280
rs11066280
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03
High density lipoprotein measurement
0.700 1.000 1 2017 2017
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: 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: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.700 1.000 1 2014 2014
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
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
Serum gamma-glutamyl transferase 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
Diabetes Mellitus, Non-Insulin-Dependent
0.810 1.000 1 2013 2016
dbSNP: rs2074356
rs2074356
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.700 1.000 1 2018 2018