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.
ASTHMA, SUSCEPTIBILITY TO (finding)
CUI: C1869116
Disease: ASTHMA, SUSCEPTIBILITY TO (finding)
3 0.695 0.400 2 138002079 missense variant C/T snv 1.0E-01 8.4E-02 0.700 0
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.695 0.400 2 138002079 missense variant C/T snv 1.0E-01 8.4E-02 0.070 0.857 7 2008 2017
Alcoholic Intoxication, Chronic
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
441 0.695 0.400 2 138002079 missense variant C/T snv 1.0E-01 8.4E-02 0.030 0.667 3 2005 2011
Asthma
CUI: C0004096
Disease: Asthma
1536 0.695 0.400 2 138002079 missense variant C/T snv 1.0E-01 8.4E-02 0.030 1.000 3 2005 2011
Essential Tremor
CUI: C0270736
Disease: Essential Tremor
79 0.695 0.400 2 138002079 missense variant C/T snv 1.0E-01 8.4E-02 0.020 1.000 2 2008 2010
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.695 0.400 2 138002079 missense variant C/T snv 1.0E-01 8.4E-02 0.010 1.000 1 2011 2011
Amyotrophic Lateral Sclerosis
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
485 0.695 0.400 2 138002079 missense variant C/T snv 1.0E-01 8.4E-02 0.010 1.000 1 2018 2018
Anxious personality
CUI: C0860602
Disease: Anxious personality
2 0.695 0.400 2 138002079 missense variant C/T snv 1.0E-01 8.4E-02 0.010 1.000 1 2005 2005
Attention deficit hyperactivity disorder
420 0.695 0.400 2 138002079 missense variant C/T snv 1.0E-01 8.4E-02 0.010 1.000 1 2011 2011
Chronic urticaria
CUI: C0263338
Disease: Chronic urticaria
2 0.695 0.400 2 138002079 missense variant C/T snv 1.0E-01 8.4E-02 0.010 1 2009 2009
Dermatitis, Atopic
CUI: C0011615
Disease: Dermatitis, Atopic
232 0.695 0.400 2 138002079 missense variant C/T snv 1.0E-01 8.4E-02 0.010 1.000 1 2008 2008
Duodenal Ulcer
CUI: C0013295
Disease: Duodenal Ulcer
33 0.695 0.400 2 138002079 missense variant C/T snv 1.0E-01 8.4E-02 0.010 1.000 1 2008 2008
Eczema
CUI: C0013595
Disease: Eczema
368 0.695 0.400 2 138002079 missense variant C/T snv 1.0E-01 8.4E-02 0.010 1.000 1 2008 2008
Migraine Disorders
CUI: C0149931
Disease: Migraine Disorders
264 0.695 0.400 2 138002079 missense variant C/T snv 1.0E-01 8.4E-02 0.010 1.000 1 2017 2017
Movement Disorders
CUI: C0026650
Disease: Movement Disorders
247 0.695 0.400 2 138002079 missense variant C/T snv 1.0E-01 8.4E-02 0.010 1.000 1 2008 2008
Myasthenia Gravis
CUI: C0026896
Disease: Myasthenia Gravis
93 0.695 0.400 2 138002079 missense variant C/T snv 1.0E-01 8.4E-02 0.010 1.000 1 2013 2013
Restless Legs Syndrome
CUI: C0035258
Disease: Restless Legs Syndrome
72 0.695 0.400 2 138002079 missense variant C/T snv 1.0E-01 8.4E-02 0.010 1.000 1 2017 2017
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
2897 0.695 0.400 2 138002079 missense variant C/T snv 1.0E-01 8.4E-02 0.010 1.000 1 2015 2015
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
827 0.695 0.400 2 138002079 missense variant C/T snv 1.0E-01 8.4E-02 0.010 1.000 1 2006 2006