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: rs1801133
rs1801133
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27
CUI: C0033975
Disease: Psychotic Disorders
Psychotic Disorders
0.010 1.000 1 2017 2017
dbSNP: rs1801133
rs1801133
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma
0.010 1.000 1 2017 2017
dbSNP: rs1801133
rs1801133
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27
CUI: C0264657
Disease: Renal sclerosis with hypertension
Renal sclerosis with hypertension
0.010 1.000 1 2012 2012
dbSNP: rs1801133
rs1801133
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27
VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding)
0.010 1.000 1 2014 2014
dbSNP: rs1801133
rs1801133
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27
CUI: C0280252
Disease: stage, colon cancer
stage, colon cancer
0.010 1.000 1 2014 2014
dbSNP: rs1801133
rs1801133
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27
CUI: C0853193
Disease: Bipolar I disorder
Bipolar I disorder
0.010 1.000 1 2016 2016
dbSNP: rs1801133
rs1801133
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.010 1.000 1 2014 2014
dbSNP: rs1801133
rs1801133
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27
CUI: C0700095
Disease: Central neuroblastoma
Central neuroblastoma
0.010 1.000 1 2015 2015
dbSNP: rs1801133
rs1801133
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27
CUI: C0009088
Disease: Cluster Headache
Cluster Headache
0.010 < 0.001 1 2011 2011
dbSNP: rs1801133
rs1801133
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27
CUI: C0521158
Disease: Recurrent tumor
Recurrent tumor
0.010 1.000 1 2014 2014
dbSNP: rs1801133
rs1801133
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27
CUI: C0079744
Disease: Diffuse Large B-Cell Lymphoma
Diffuse Large B-Cell Lymphoma
0.010 1.000 1 2014 2014
dbSNP: rs1801133
rs1801133
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27
CUI: C0002902
Disease: Anencephaly
Anencephaly
0.010 1.000 1 2015 2015
dbSNP: rs1801133
rs1801133
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27
CUI: C0852733
Disease: Completed Suicide
Completed Suicide
0.010 1.000 1 2012 2012
dbSNP: rs1801133
rs1801133
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.010 1.000 1 2013 2013
dbSNP: rs1801133
rs1801133
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27
CUI: C0522254
Disease: Analgesic Overuse Headache
Analgesic Overuse Headache
0.010 1.000 1 2013 2013
dbSNP: rs1801133
rs1801133
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27
CUI: C0023473
Disease: Myeloid Leukemia, Chronic
Myeloid Leukemia, Chronic
0.010 1.000 1 2014 2014
dbSNP: rs1801133
rs1801133
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma
0.010 1.000 1 2017 2017
dbSNP: rs1801133
rs1801133
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27
Methylenetetrahydrofolate reductase deficiency
0.010 1.000 1 2014 2014
dbSNP: rs1801133
rs1801133
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27
CUI: C0011847
Disease: Diabetes
Diabetes
0.010 1.000 1 2013 2013
dbSNP: rs1801133
rs1801133
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia
0.010 1.000 1 2018 2018
dbSNP: rs1801133
rs1801133
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27
CUI: C0039685
Disease: Tetralogy of Fallot
Tetralogy of Fallot
0.010 1.000 1 2012 2012
dbSNP: rs1801133
rs1801133
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27
CUI: C0017636
Disease: Glioblastoma
Glioblastoma
0.010 1.000 1 2008 2008
dbSNP: rs1801133
rs1801133
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27
CUI: C0018799
Disease: Heart Diseases
Heart Diseases
0.010 1.000 1 2014 2014
dbSNP: rs1801133
rs1801133
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27
CUI: C0021125
Disease: Impulsive Behavior
Impulsive Behavior
0.010 1.000 1 2017 2017
dbSNP: rs1801133
rs1801133
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27
CUI: C0002878
Disease: Anemia, Hemolytic
Anemia, Hemolytic
0.010 1.000 1 2002 2002