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
0.821 0.214 12 112207597 intron variant G/A snp 8.6E-03
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.810 < 0.001 1 2014 2016
dbSNP: rs2074356
rs2074356
HECTD4
0.821 0.214 12 112207597 intron variant G/A snp 8.6E-03
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.800 2 2011 2017
dbSNP: rs11066280
rs11066280
HECTD4
0.769 0.214 12 112379979 intron variant T/A snp 1.5E-02
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma 		0.800 1 2011 2011
dbSNP: rs11066280
rs11066280
HECTD4
0.769 0.214 12 112379979 intron variant T/A snp 1.5E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.800 1 2012 2013
dbSNP: rs11066280
rs11066280
HECTD4
0.769 0.214 12 112379979 intron variant T/A snp 1.5E-02
CUI: C0013124
Disease: Drinking behavior processes
Drinking behavior processes 		0.800 1 2013 2013
dbSNP: rs2074356
rs2074356
HECTD4
0.821 0.214 12 112207597 intron variant G/A snp 8.6E-03
CUI: C0005845
Disease: Blood urea nitrogen measurement
Blood urea nitrogen measurement 		0.800 1 2012 2012
dbSNP: rs2074356
rs2074356
HECTD4
0.821 0.214 12 112207597 intron variant G/A snp 8.6E-03
CUI: C1278049
Disease: Serum gamma-glutamyl transferase measurement
Serum gamma-glutamyl transferase measurement 		0.800 1 2011 2011
dbSNP: rs2074356
rs2074356
HECTD4
0.821 0.214 12 112207597 intron variant G/A snp 8.6E-03
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1 2011 2011
dbSNP: rs2074356
rs2074356
HECTD4
0.821 0.214 12 112207597 intron variant G/A snp 8.6E-03
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma 		0.800 1 2011 2011
dbSNP: rs11066280
rs11066280
HECTD4
0.769 0.214 12 112379979 intron variant T/A snp 1.5E-02
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.710 1.000 1 2014 2015
dbSNP: rs11066280
rs11066280
HECTD4
0.769 0.214 12 112379979 intron variant T/A snp 1.5E-02
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 3 2011 2016
dbSNP: rs11066280
rs11066280
HECTD4
0.769 0.214 12 112379979 intron variant T/A snp 1.5E-02
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 3 2011 2016
dbSNP: rs11066280
rs11066280
HECTD4
0.769 0.214 12 112379979 intron variant T/A snp 1.5E-02
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1 2017 2017
dbSNP: rs11066280
rs11066280
HECTD4
0.769 0.214 12 112379979 intron variant T/A snp 1.5E-02
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		0.700 1 2014 2014
dbSNP: rs11066280
rs11066280
HECTD4
0.769 0.214 12 112379979 intron variant T/A snp 1.5E-02
CUI: C1883008
Disease: Serum Alanine Aminotransferase Measurement
Serum Alanine Aminotransferase Measurement 		0.700 1 2011 2011
dbSNP: rs11066280
rs11066280
HECTD4
0.769 0.214 12 112379979 intron variant T/A snp 1.5E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1 2016 2016
dbSNP: rs2074356
rs2074356
HECTD4
0.821 0.214 12 112207597 intron variant G/A snp 8.6E-03
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1 2017 2017
dbSNP: rs2074356
rs2074356
HECTD4
0.821 0.214 12 112207597 intron variant G/A snp 8.6E-03
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1 2009 2009
dbSNP: rs2285810
rs2285810
HECTD4
12 112261736 non coding transcript exon variant T/C snp 0.45
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement 		0.700 1 2017 2017
dbSNP: rs2285810
rs2285810
HECTD4
12 112261736 non coding transcript exon variant T/C snp 0.45
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1 2017 2017
dbSNP: rs2301712
rs2301712
HECTD4
12 112203573 non coding transcript exon variant T/G snp 0.10 9.6E-02
CUI: C0578022
Disease: Finding of body mass index
Finding of body mass index 		0.700 1 2017 2017
dbSNP: rs2301712
rs2301712
HECTD4
12 112203573 non coding transcript exon variant T/G snp 0.10 9.6E-02
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1 2017 2017
dbSNP: rs555346412
rs555346412
HECTD4
12 112191863 intron variant G/C snp 6.7E-04
CUI: C0857490
Disease: Granulocyte count
Granulocyte count 		0.700 1 2017 2017
dbSNP: rs555346412
rs555346412
HECTD4
12 112191863 intron variant G/C snp 6.7E-04
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1 2017 2017
dbSNP: rs555346412
rs555346412
HECTD4
12 112191863 intron variant G/C snp 6.7E-04
CUI: C0750879
Disease: Eosinophil count result
Eosinophil count result 		0.700 1 2017 2017