Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs9371533
rs9371533
0.925 0.120 6 149889545 missense variant G/A;C snv 0.52
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs6925151
rs6925151
1.000 0.040 6 149889587 missense variant C/T snv 0.29 0.30
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.010 1.000 1 2018 2018
dbSNP: rs7756850
rs7756850
0.925 0.120 6 149891460 intron variant G/C snv 0.40
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.010 1.000 1 2018 2018
dbSNP: rs7756850
rs7756850
0.925 0.120 6 149891460 intron variant G/C snv 0.40
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs9371533
rs9371533
0.925 0.120 6 149889545 missense variant G/A;C snv 0.52
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs9371533
rs9371533
0.925 0.120 6 149889545 missense variant G/A;C snv 0.52
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.010 1.000 1 2018 2018
dbSNP: rs9383921
rs9383921
0.925 0.120 6 149889549 missense variant C/T snv 0.45 0.36
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs9383921
rs9383921
0.925 0.120 6 149889549 missense variant C/T snv 0.45 0.36
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.010 1.000 1 2018 2018