Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Diabetes Mellitus, Non-Insulin-Dependent
1522 0.596 0.536 10 112998590 intron variant C/G,T snp 0.26 0.900 0.920 138 2006 2017
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
440 0.596 0.536 10 112998590 intron variant C/G,T snp 0.26 0.100 0.964 28 2006 2018
Diabetes
CUI: C0011847
Disease: Diabetes
349 0.596 0.536 10 112998590 intron variant C/G,T snp 0.26 0.100 0.962 26 2006 2018
Obesity
CUI: C0028754
Disease: Obesity
811 0.596 0.536 10 112998590 intron variant C/G,T snp 0.26 0.080 1.000 8 2008 2017
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
293 0.596 0.536 10 112998590 intron variant C/G,T snp 0.26 0.850 0.800 6 2009 2012
Body mass index
CUI: C1305855
Disease: Body mass index
1022 0.596 0.536 10 112998590 intron variant C/G,T snp 0.26 0.700 5 2012 2017
Finding of body mass index
CUI: C0578022
Disease: Finding of body mass index
1022 0.596 0.536 10 112998590 intron variant C/G,T snp 0.26 0.700 5 2012 2017
Hyperglycemia
CUI: C0020456
Disease: Hyperglycemia
37 0.596 0.536 10 112998590 intron variant C/G,T snp 0.26 0.050 1.000 5 2007 2012
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
197 0.596 0.536 10 112998590 intron variant C/G,T snp 0.26 0.040 0.750 4 2008 2018
Latent autoimmune diabetes mellitus in adult
8 0.596 0.536 10 112998590 intron variant C/G,T snp 0.26 0.040 1.000 4 2008 2015
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
121 0.596 0.536 10 112998590 intron variant C/G,T snp 0.26 0.030 0.667 3 2008 2010
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
131 0.596 0.536 10 112998590 intron variant C/G,T snp 0.26 0.030 0.667 3 2008 2010
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
135 0.596 0.536 10 112998590 intron variant C/G,T snp 0.26 0.030 1.000 3 2008 2014
Polycystic Ovary Syndrome
CUI: C0032460
Disease: Polycystic Ovary Syndrome
181 0.596 0.536 10 112998590 intron variant C/G,T snp 0.26 0.030 0.333 3 2008 2016
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
1839 0.596 0.536 10 112998590 intron variant C/G,T snp 0.26 0.020 1.000 2 2013 2016
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
331 0.596 0.536 10 112998590 intron variant C/G,T snp 0.26 0.020 1.000 2 2014 2015
Colon Carcinoma
CUI: C0699790
Disease: Colon Carcinoma
240 0.596 0.536 10 112998590 intron variant C/G,T snp 0.26 0.020 1.000 2 2008 2008
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
861 0.596 0.536 10 112998590 intron variant C/G,T snp 0.26 0.020 1.000 2 2010 2011
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
760 0.596 0.536 10 112998590 intron variant C/G,T snp 0.26 0.710 1.000 2 2010 2011
Fasting blood glucose measurement
CUI: C0428568
Disease: Fasting blood glucose measurement
87 0.596 0.536 10 112998590 intron variant C/G,T snp 0.26 0.800 2 2009 2012
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
1365 0.596 0.536 10 112998590 intron variant C/G,T snp 0.26 0.020 1.000 2 2013 2016
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
563 0.596 0.536 10 112998590 intron variant C/G,T snp 0.26 0.020 1.000 2 2010 2014
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
756 0.596 0.536 10 112998590 intron variant C/G,T snp 0.26 0.020 1.000 2 2010 2014
Autoantibody measurement
CUI: C1272321
Disease: Autoantibody measurement
8 0.596 0.536 10 112998590 intron variant C/G,T snp 0.26 0.700 1 2009 2009
Autonomic neuropathy
CUI: C0259749
Disease: Autonomic neuropathy
2 0.596 0.536 10 112998590 intron variant C/G,T snp 0.26 0.010 1.000 1 2014 2014