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.
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
447 0.475 0.679 6 26090951 missense variant C/G snp 0.11 9.9E-02 0.810 1.000 2 2012 2013
HEMOCHROMATOSIS, TYPE 1
CUI: C3469186
Disease: HEMOCHROMATOSIS, TYPE 1
42 0.475 0.679 6 26090951 missense variant C/G snp 0.11 9.9E-02 0.800 0.923 81 1993 2017
Hereditary hemochromatosis
CUI: C0392514
Disease: Hereditary hemochromatosis
36 0.475 0.679 6 26090951 missense variant C/G snp 0.11 9.9E-02 0.800 0.922 73 1993 2017
Hemoglobin measurement
CUI: C0518015
Disease: Hemoglobin measurement
219 0.475 0.679 6 26090951 missense variant C/G snp 0.11 9.9E-02 0.800 2 2009 2017
Mean corpuscular hemoglobin concentration determination
583 0.475 0.679 6 26090951 missense variant C/G snp 0.11 9.9E-02 0.800 2 2009 2017
MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 7 (finding)
1 0.475 0.679 6 26090951 missense variant C/G snp 0.11 9.9E-02 0.700 12 1996 2008
Blood Pressure
CUI: C0005823
Disease: Blood Pressure
223 0.475 0.679 6 26090951 missense variant C/G snp 0.11 9.9E-02 0.700 3 2011 2012
Blood pressure finding
CUI: C1271104
Disease: Blood pressure finding
223 0.475 0.679 6 26090951 missense variant C/G snp 0.11 9.9E-02 0.700 3 2011 2012
Systemic arterial pressure
CUI: C1272641
Disease: Systemic arterial pressure
223 0.475 0.679 6 26090951 missense variant C/G snp 0.11 9.9E-02 0.700 3 2011 2012
Diastolic blood pressure
CUI: C0428883
Disease: Diastolic blood pressure
256 0.475 0.679 6 26090951 missense variant C/G snp 0.11 9.9E-02 0.700 2 2012 2017
Serum iron measurement
CUI: C1318312
Disease: Serum iron measurement
24 0.475 0.679 6 26090951 missense variant C/G snp 0.11 9.9E-02 0.700 2 2011 2017
Systolic Pressure
CUI: C0871470
Disease: Systolic Pressure
244 0.475 0.679 6 26090951 missense variant C/G snp 0.11 9.9E-02 0.700 2 2012 2017
Erythrocyte Mean Corpuscular Hemoglobin Test
4531 0.475 0.679 6 26090951 missense variant C/G snp 0.11 9.9E-02 0.700 1 2012 2012
Ferritin measurement
CUI: C0373607
Disease: Ferritin measurement
155 0.475 0.679 6 26090951 missense variant C/G snp 0.11 9.9E-02 0.700 1 2017 2017
Finding of Mean Corpuscular Hemoglobin
4531 0.475 0.679 6 26090951 missense variant C/G snp 0.11 9.9E-02 0.700 1 2012 2012
Hematocrit procedure
CUI: C0018935
Disease: Hematocrit procedure
212 0.475 0.679 6 26090951 missense variant C/G snp 0.11 9.9E-02 0.700 1 2017 2017
Platelet Count measurement
CUI: C0032181
Disease: Platelet Count measurement
353 0.475 0.679 6 26090951 missense variant C/G snp 0.11 9.9E-02 0.700 1 2017 2017
Reticulocyte count (procedure)
CUI: C0206161
Disease: Reticulocyte count (procedure)
472 0.475 0.679 6 26090951 missense variant C/G snp 0.11 9.9E-02 0.700 1 2017 2017
Transferrin saturation measurement
CUI: C1277709
Disease: Transferrin saturation measurement
33 0.475 0.679 6 26090951 missense variant C/G snp 0.11 9.9E-02 0.700 1 2017 2017
Unsaturated iron binding capacity measurement
33 0.475 0.679 6 26090951 missense variant C/G snp 0.11 9.9E-02 0.700 1 2017 2017
Hemochromatosis
CUI: C0018995
Disease: Hemochromatosis
22 0.475 0.679 6 26090951 missense variant C/G snp 0.11 9.9E-02 0.100 0.941 51 1997 2016
Iron Overload
CUI: C0282193
Disease: Iron Overload
30 0.475 0.679 6 26090951 missense variant C/G snp 0.11 9.9E-02 0.100 0.755 49 1997 2016
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1062 0.475 0.679 6 26090951 missense variant C/G snp 0.11 9.9E-02 0.100 0.917 12 2003 2016
Amyotrophic Lateral Sclerosis
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
259 0.475 0.679 6 26090951 missense variant C/G snp 0.11 9.9E-02 0.080 0.750 8 2007 2016
Cirrhosis
CUI: C1623038
Disease: Cirrhosis
48 0.475 0.679 6 26090951 missense variant C/G snp 0.11 9.9E-02 0.080 0.875 8 2001 2005