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.
Adiponectin Measurement
CUI: C2700366
Disease: Adiponectin Measurement
70 0.763 0.440 3 186853407 intron variant A/G snv 0.10 0.700 1.000 1 2010 2010
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.763 0.440 3 186853407 intron variant A/G snv 0.10 0.010 1.000 1 2012 2012
Diabetic Nephropathy
CUI: C0011881
Disease: Diabetic Nephropathy
238 0.763 0.440 3 186853407 intron variant A/G snv 0.10 0.010 1.000 1 2014 2014
Generalized obesity
CUI: C0342942
Disease: Generalized obesity
4 0.763 0.440 3 186853407 intron variant A/G snv 0.10 0.010 1.000 1 2013 2013
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.763 0.440 3 186853407 intron variant A/G snv 0.10 0.010 1.000 1 2017 2017
Large-artery atherosclerosis (embolus/thrombosis)
CUI: C4699512
Disease: Large-artery atherosclerosis (embolus/thrombosis)
35 0.763 0.440 3 186853407 intron variant A/G snv 0.10 0.010 1.000 1 2017 2017
Non-alcoholic Fatty Liver Disease
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
222 0.763 0.440 3 186853407 intron variant A/G snv 0.10 0.010 1.000 1 2015 2015
Polycystic Ovary Syndrome
CUI: C0032460
Disease: Polycystic Ovary Syndrome
363 0.763 0.440 3 186853407 intron variant A/G snv 0.10 0.010 1.000 1 2020 2020
skin fold (abnormality)
CUI: C1399793
Disease: skin fold (abnormality)
8 0.763 0.440 3 186853407 intron variant A/G snv 0.10 0.010 1.000 1 2006 2006
Splenic Hypoplasia
CUI: C0685889
Disease: Splenic Hypoplasia
9 0.763 0.440 3 186853407 intron variant A/G snv 0.10 0.010 1.000 1 2017 2017