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.
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
293 0.846 0.107 2 168906638 intron variant T/C snp 0.79 0.79 0.810 1.000 2 2009 2012
Fasting blood glucose measurement
CUI: C0428568
Disease: Fasting blood glucose measurement
87 0.846 0.107 2 168906638 intron variant T/C snp 0.79 0.79 0.800 6 2008 2017
Calcification of coronary artery
CUI: C1611184
Disease: Calcification of coronary artery
3393 0.846 0.107 2 168906638 intron variant T/C snp 0.79 0.79 0.800 2 2012 2012
Glucose measurement
CUI: C0337438
Disease: Glucose measurement
89 0.846 0.107 2 168906638 intron variant T/C snp 0.79 0.79 0.800 1 2009 2009
Finding of body mass index
CUI: C0578022
Disease: Finding of body mass index
1022 0.846 0.107 2 168906638 intron variant T/C snp 0.79 0.79 0.700 1 2012 2012
Protein measurement
CUI: C0202202
Disease: Protein measurement
422 0.846 0.107 2 168906638 intron variant T/C snp 0.79 0.79 0.700 1 2016 2016
Body mass index
CUI: C1305855
Disease: Body mass index
1022 0.846 0.107 2 168906638 intron variant T/C snp 0.79 0.79 0.700 1 2012 2012
Amino acids measurement
CUI: C0201874
Disease: Amino acids measurement
42 0.846 0.107 2 168906638 intron variant T/C snp 0.79 0.79 0.700 1 2016 2016
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
440 0.846 0.107 2 168906638 intron variant T/C snp 0.79 0.79 0.020 1.000 2 2013 2013
Diabetes
CUI: C0011847
Disease: Diabetes
349 0.846 0.107 2 168906638 intron variant T/C snp 0.79 0.79 0.020 1.000 2 2013 2013
Diabetes Mellitus, Non-Insulin-Dependent
1522 0.846 0.107 2 168906638 intron variant T/C snp 0.79 0.79 0.020 1.000 2 2009 2014
Impaired glucose tolerance
CUI: C0271650
Disease: Impaired glucose tolerance
55 0.846 0.107 2 168906638 intron variant T/C snp 0.79 0.79 0.020 1.000 2 2009 2011
Obesity
CUI: C0028754
Disease: Obesity
811 0.846 0.107 2 168906638 intron variant T/C snp 0.79 0.79 0.010 1.000 1 2015 2015