rs4918, AHSG

N. diseases: 12
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
CUI: C0011849
Disease: Diabetes Mellitus
824 0.763 0.400 3 186620593 missense variant G/A;C snv 0.67 0.020 1.000 2 2005 2016
Obesity
CUI: C0028754
Disease: Obesity
1111 0.763 0.400 3 186620593 missense variant G/A;C snv 0.67 0.020 1.000 2 2005 2016
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.763 0.400 3 186620593 missense variant G/A;C snv 0.67 0.010 1.000 1 2005 2005
Cerebral Infarction
CUI: C0007785
Disease: Cerebral Infarction
123 0.763 0.400 3 186620593 missense variant G/A;C snv 0.67 0.010 1.000 1 2013 2013
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.763 0.400 3 186620593 missense variant G/A;C snv 0.67 0.010 1.000 1 2016 2016
Hodgkin Disease
CUI: C0019829
Disease: Hodgkin Disease
148 0.763 0.400 3 186620593 missense variant G/A;C snv 0.67 0.010 1 2007 2007
Huntington Disease
CUI: C0020179
Disease: Huntington Disease
115 0.763 0.400 3 186620593 missense variant G/A;C snv 0.67 0.010 1 2007 2007
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.763 0.400 3 186620593 missense variant G/A;C snv 0.67 0.010 1.000 1 2013 2013
Malnutrition
CUI: C0162429
Disease: Malnutrition
29 0.763 0.400 3 186620593 missense variant G/A;C snv 0.67 0.010 1.000 1 2005 2005
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.763 0.400 3 186620593 missense variant G/A;C snv 0.67 0.010 1.000 1 2008 2008
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.763 0.400 3 186620593 missense variant G/A;C snv 0.67 0.010 1.000 1 2016 2016
Vascular calcification
CUI: C0342649
Disease: Vascular calcification
3 0.763 0.400 3 186620593 missense variant G/A;C snv 0.67 0.010 1.000 1 2009 2009