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: rs555346412
rs555346412
HECTD4
12 112191863 intron variant G/C snv 8.2E-04
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs77768175
rs77768175
HECTD4
1.000 0.040 12 112298314 intron variant A/G snv 5.8E-03
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2019 2019
dbSNP: rs7953257
rs7953257
HECTD4
12 112246417 intron variant A/G;T snv 0.71
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.700 1.000 1 2018 2018
dbSNP: rs7953257
rs7953257
HECTD4
12 112246417 intron variant A/G;T snv 0.71
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2018 2018
dbSNP: rs7953257
rs7953257
HECTD4
12 112246417 intron variant A/G;T snv 0.71
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure 		0.700 1.000 1 2018 2018
dbSNP: rs7953257
rs7953257
HECTD4
12 112246417 intron variant A/G;T snv 0.71
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2018 2018
dbSNP: rs7953257
rs7953257
HECTD4
12 112246417 intron variant A/G;T snv 0.71
CUI: C1305849
Disease: Diastolic blood pressure measurement
Diastolic blood pressure measurement 		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: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.710 1.000 1 2014 2015
dbSNP: rs2074356
rs2074356
HECTD4
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 2 2011 2019
dbSNP: rs2074356
rs2074356
HECTD4
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
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: 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