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 0.679 0.357 10 113049143 intron variant G/A,T snp 0.24 0.900 0.894 53 2006 2017
Diabetes
CUI: C0011847
Disease: Diabetes
349 0.679 0.357 10 113049143 intron variant G/A,T snp 0.24 0.070 1.000 7 2006 2015
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
440 0.679 0.357 10 113049143 intron variant G/A,T snp 0.24 0.070 1.000 7 2006 2015
Impaired glucose tolerance
CUI: C0271650
Disease: Impaired glucose tolerance
55 0.679 0.357 10 113049143 intron variant G/A,T snp 0.24 0.020 1.000 2 2006 2006
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
293 0.679 0.357 10 113049143 intron variant G/A,T snp 0.24 0.020 0.500 2 2009 2011
Breast Cancer, Familial
CUI: C0346153
Disease: Breast Cancer, Familial
705 0.679 0.357 10 113049143 intron variant G/A,T snp 0.24 0.010 1.000 1 2006 2006
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
1839 0.679 0.357 10 113049143 intron variant G/A,T snp 0.24 0.010 1.000 1 2008 2008
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
861 0.679 0.357 10 113049143 intron variant G/A,T snp 0.24 0.010 1.000 1 2011 2011
Diabetes in youth
CUI: C3825462
Disease: Diabetes in youth
2 0.679 0.357 10 113049143 intron variant G/A,T snp 0.24 0.010 1.000 1 2011 2011
Diabetes Mellitus, Insulin-Dependent
775 0.679 0.357 10 113049143 intron variant G/A,T snp 0.24 0.010 1.000 1 2011 2011
Hyperlipidemia, Familial Combined
CUI: C0020474
Disease: Hyperlipidemia, Familial Combined
20 0.679 0.357 10 113049143 intron variant G/A,T snp 0.24 0.010 1.000 1 2008 2008
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
1365 0.679 0.357 10 113049143 intron variant G/A,T snp 0.24 0.010 1.000 1 2008 2008
Malignant neoplasm of ovary
CUI: C1140680
Disease: Malignant neoplasm of ovary
244 0.679 0.357 10 113049143 intron variant G/A,T snp 0.24 0.010 1 2009 2009
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
563 0.679 0.357 10 113049143 intron variant G/A,T snp 0.24 0.010 1.000 1 2008 2008
Obesity
CUI: C0028754
Disease: Obesity
811 0.679 0.357 10 113049143 intron variant G/A,T snp 0.24 0.010 1.000 1 2009 2009
Ovarian Carcinoma
CUI: C0029925
Disease: Ovarian Carcinoma
316 0.679 0.357 10 113049143 intron variant G/A,T snp 0.24 0.010 1 2009 2009
Polycystic Ovary Syndrome
CUI: C0032460
Disease: Polycystic Ovary Syndrome
181 0.679 0.357 10 113049143 intron variant G/A,T snp 0.24 0.010 1.000 1 2016 2016
Prediabetes syndrome
CUI: C0362046
Disease: Prediabetes syndrome
14 0.679 0.357 10 113049143 intron variant G/A,T snp 0.24 0.010 1.000 1 2008 2008
Premature adrenarche
CUI: C0342546
Disease: Premature adrenarche
3 0.679 0.357 10 113049143 intron variant G/A,T snp 0.24 0.010 1 2009 2009
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
756 0.679 0.357 10 113049143 intron variant G/A,T snp 0.24 0.010 1.000 1 2008 2008