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: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
Diabetes Mellitus, Non-Insulin-Dependent
0.900 1.000 3 2007 2018
dbSNP: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.830 1.000 3 2010 2018
dbSNP: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.810 1.000 1 2010 2016
dbSNP: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 9 2007 2019
dbSNP: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
CUI: C0428568
Disease: Fasting blood glucose measurement
Fasting blood glucose measurement
0.800 1.000 6 2010 2019
dbSNP: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
CUI: C1305855
Disease: Body mass index
Body mass index
0.800 1.000 3 2012 2019
dbSNP: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 3 2012 2019
dbSNP: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
Low density lipoprotein cholesterol measurement
0.800 1.000 3 2008 2019
dbSNP: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
CUI: C0495706
Disease: elevated blood glucose level
elevated blood glucose level
0.800 1.000 2 2011 2018
dbSNP: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.800 1.000 2 2008 2019
dbSNP: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure)
0.800 1.000 2 2009 2015
dbSNP: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
CUI: C0337438
Disease: Glucose measurement
Glucose measurement
0.800 1.000 2 2011 2018
dbSNP: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty
0.800 1.000 1 2010 2017
dbSNP: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 1.000 1 2008 2015
dbSNP: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
CUI: C0018099
Disease: Gout
Gout
0.800 1.000 1 2010 2017
dbSNP: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
CUI: C0201925
Disease: Calcium measurement
Calcium measurement
0.800 1.000 1 2013 2013
dbSNP: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
Non-alcoholic Fatty Liver Disease
0.790 1.000 1 2011 2019
dbSNP: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.740 1.000 1 2010 2016
dbSNP: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
CUI: C0011847
Disease: Diabetes
Diabetes
0.740 1.000 1 2010 2016
dbSNP: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia
0.730 1.000 1 2010 2017
dbSNP: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident
0.710 1.000 1 2010 2016
dbSNP: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2014 2014
dbSNP: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption
0.700 1.000 1 2017 2017
dbSNP: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
High density lipoprotein measurement
0.700 1.000 1 2016 2016
dbSNP: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2016 2016