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
HECTD4
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
HECTD4
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
HECTD4
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
HECTD4
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
HECTD4
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
HECTD4
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
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03
CUI: C0201836
Disease: Alanine aminotransferase measurement
Alanine aminotransferase measurement 		0.700 1.000 2 2011 2019
dbSNP: rs11066280
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03
CUI: C1883008
Disease: Serum Alanine Aminotransferase Measurement
Serum Alanine Aminotransferase Measurement 		0.700 1.000 2 2011 2019
dbSNP: rs11066280
rs11066280
HECTD4
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
HECTD4
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: rs11066280
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2017 2017
dbSNP: rs11066280
rs11066280
HECTD4
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
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03
CUI: C0201899
Disease: Aspartate aminotransferase measurement
Aspartate aminotransferase measurement 		0.700 1.000 1 2019 2019