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: rs2074356
rs2074356
HECTD4
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.810 1.000 1 2013 2016
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: 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: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms 		0.800 1.000 1 2010 2011
dbSNP: rs2074356
rs2074356
HECTD4
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
HECTD4
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
HECTD4
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: 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: rs1005902
rs1005902
HECTD4
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
HECTD4
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
HECTD4
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
HECTD4
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
HECTD4
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
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: C0201899
Disease: Aspartate aminotransferase measurement
Aspartate aminotransferase measurement 		0.700 1.000 1 2019 2019
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: 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: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		0.700 1.000 1 2014 2014
dbSNP: rs2074356
rs2074356
HECTD4
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03
CUI: C1278049
Disease: Serum gamma-glutamyl transferase measurement
Serum gamma-glutamyl transferase measurement 		0.700 1.000 1 2011 2011
dbSNP: rs2074356
rs2074356
HECTD4
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
dbSNP: rs2074356
rs2074356
HECTD4
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2017 2017
dbSNP: rs2285810
rs2285810
HECTD4
12 112261736 non coding transcript exon variant T/C snv 0.45
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement 		0.700 1.000 1 2016 2016
dbSNP: rs2285810
rs2285810
HECTD4
12 112261736 non coding transcript exon variant T/C snv 0.45
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2016 2016
dbSNP: rs2301712
rs2301712
HECTD4
12 112203573 non coding transcript exon variant T/G snv 0.10 9.1E-02
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2017 2017
dbSNP: rs4766898
rs4766898
HECTD4
12 112344040 intron variant C/T snv 4.8E-02
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure) 		0.700 1.000 1 2019 2019