rs560887, SPC25;G6PC2

N. diseases: 11
Source: INFERRED ×
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
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 0.820 1.000 1 2009 2017
Fasting blood glucose measurement
CUI: C0428568
Disease: Fasting blood glucose measurement
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 0.800 1.000 9 2008 2019
Body mass index
CUI: C1305855
Disease: Body mass index
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 0.800 1.000 1 2012 2012
elevated blood glucose level
CUI: C0495706
Disease: elevated blood glucose level
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 0.800 1.000 1 2009 2009
Glucose measurement
CUI: C0337438
Disease: Glucose measurement
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 0.800 1.000 1 2009 2009
Amino acids measurement
CUI: C0201874
Disease: Amino acids measurement
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 0.700 1.000 1 2016 2016
Birth Weight
CUI: C0005612
Disease: Birth Weight
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 0.700 1.000 1 2019 2019
Calcification of coronary artery
CUI: C1611184
Disease: Calcification of coronary artery
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 0.700 1.000 1 2012 2012
Fasting blood sugar result
CUI: C1261430
Disease: Fasting blood sugar result
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 0.700 1.000 1 2012 2012
Protein measurement
CUI: C0202202
Disease: Protein measurement
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 0.700 1.000 1 2016 2016
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 0.700 1.000 1 2012 2012