Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1800587
rs1800587
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis
0.030 1.000 3 2011 2019
dbSNP: rs1800587
rs1800587
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.030 0.667 3 2009 2013
dbSNP: rs1800587
rs1800587
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32
CUI: C0339143
Disease: Thyroid associated opthalmopathies
Thyroid associated opthalmopathies
0.020 1.000 2 2010 2015
dbSNP: rs1800587
rs1800587
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32
CUI: C0030193
Disease: Pain
Pain
0.020 1.000 2 2014 2016
dbSNP: rs1800587
rs1800587
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32
CUI: C0018213
Disease: Graves Disease
Graves Disease
0.020 1.000 2 2010 2018
dbSNP: rs1800587
rs1800587
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32
CUI: C0011265
Disease: Presenile dementia
Presenile dementia
0.020 1.000 2 2012 2013
dbSNP: rs1800587
rs1800587
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32
CUI: C0019270
Disease: Hernia
Hernia
0.020 1.000 2 2014 2014
dbSNP: rs1800587
rs1800587
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32
CUI: C0266929
Disease: Chronic Periodontitis
Chronic Periodontitis
0.020 1.000 2 2018 2019
dbSNP: rs1800587
rs1800587
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32
CUI: C0497327
Disease: Dementia
Dementia
0.020 1.000 2 2012 2013
dbSNP: rs1800587
rs1800587
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32
CUI: C0391826
Disease: Lhermitte-Duclos disease
Lhermitte-Duclos disease
0.010 1.000 1 2017 2017
dbSNP: rs1800587
rs1800587
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32
CUI: C0002895
Disease: Anemia, Sickle Cell
Anemia, Sickle Cell
0.010 1.000 1 2016 2016
dbSNP: rs1800587
rs1800587
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.010 1.000 1 2019 2019
dbSNP: rs1800587
rs1800587
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32
CUI: C0011570
Disease: Mental Depression
Mental Depression
0.010 1.000 1 2013 2013
dbSNP: rs1800587
rs1800587
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix
0.010 1.000 1 2019 2019
dbSNP: rs1800587
rs1800587
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32
CUI: C4048328
Disease: cervical cancer
cervical cancer
0.010 1.000 1 2019 2019
dbSNP: rs1800587
rs1800587
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32
Diabetes Mellitus, Insulin-Dependent
0.010 1.000 1 2016 2016
dbSNP: rs1800587
rs1800587
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32
CUI: C4275242
Disease: Sudden sensorineural hearing loss
Sudden sensorineural hearing loss
0.010 1.000 1 2011 2011
dbSNP: rs1800587
rs1800587
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32
CUI: C0041696
Disease: Unipolar Depression
Unipolar Depression
0.010 1.000 1 2013 2013
dbSNP: rs1800587
rs1800587
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.010 1.000 1 2009 2009
dbSNP: rs1800587
rs1800587
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32
CUI: C0011581
Disease: Depressive disorder
Depressive disorder
0.010 1.000 1 2013 2013
dbSNP: rs1800587
rs1800587
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32
CUI: C0278147
Disease: Radicular pain
Radicular pain
0.010 1.000 1 2014 2014
dbSNP: rs1800587
rs1800587
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder
0.010 1.000 1 2013 2013
dbSNP: rs1800587
rs1800587
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32
CUI: C0029408
Disease: Degenerative polyarthritis
Degenerative polyarthritis
0.010 1.000 1 2013 2013
dbSNP: rs1800587
rs1800587
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32
CUI: C3495798
Disease: Periodontal inflammation
Periodontal inflammation
0.010 1.000 1 2019 2019
dbSNP: rs1800587
rs1800587
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases
0.010 < 0.001 1 2018 2018