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.
Anxiety
CUI: C0003467
Disease: Anxiety
287 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.020 1.000 2 2008 2012
Anxiety Disorders
CUI: C0003469
Disease: Anxiety Disorders
163 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.020 1.000 2 2008 2012
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.030 1.000 3 2000 2008
Arthralgia
CUI: C0003862
Disease: Arthralgia
27 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.020 0.500 2 2002 2007
Arthritis
CUI: C0003864
Disease: Arthritis
69 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.080 0.875 8 2002 2019
Arthropathy
CUI: C0022408
Disease: Arthropathy
10 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.040 1.000 4 2006 2014
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.030 1.000 3 2000 2008
Autistic Disorder
CUI: C0004352
Disease: Autistic Disorder
395 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.010 1.000 1 2011 2011
Back Pain
CUI: C0004604
Disease: Back Pain
10 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.010 1.000 1 2019 2019
Barrett Esophagus
CUI: C0004763
Disease: Barrett Esophagus
60 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.010 1 2008 2008
beta Thalassemia
CUI: C0005283
Disease: beta Thalassemia
103 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.030 1.000 3 2005 2017
Beta thalassemia minor
CUI: C0869532
Disease: Beta thalassemia minor
1 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.010 1.000 1 2006 2006
Beta thalassemia trait
CUI: C0878521
Disease: Beta thalassemia trait
5 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.020 1.000 2 2005 2010
beta Thalassemia, heterozygous
CUI: C0878520
Disease: beta Thalassemia, heterozygous
2 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.010 1.000 1 2001 2001
beta^+^ Thalassemia
CUI: C3841475
Disease: beta^+^ Thalassemia
44 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.030 1.000 3 2005 2017
Brain Infarction
CUI: C0751955
Disease: Brain Infarction
11 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.010 1.000 1 2001 2001
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.060 1.000 6 2006 2015
Calcium pyrophosphate deposition disease
CUI: C0553730
Disease: Calcium pyrophosphate deposition disease
5 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.010 1 2007 2007
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.010 1.000 1 2009 2009
Carcinoma of Male Breast
CUI: C0238033
Disease: Carcinoma of Male Breast
38 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.010 1.000 1 2006 2006
Carcinoma, Ovarian Epithelial
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
327 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.010 1.000 1 2011 2011
Cardiac Arrhythmia
CUI: C0003811
Disease: Cardiac Arrhythmia
111 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.010 1.000 1 2012 2012
Cardiomyopathies
CUI: C0878544
Disease: Cardiomyopathies
294 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.020 0.500 2 1998 2001
Cardiomyopathy, Familial Idiopathic
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
243 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.010 1.000 1 2005 2005
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.030 1.000 3 2001 2008