FOXO3, forkhead box O3, 2309

N. diseases: 381; N. variants: 30
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1536057
rs1536057 		1.000 0.040 6 108564420 intron variant C/T snv 0.30
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		Mental Disorders 0.010 1.000 1 2011 2011
dbSNP: rs1935952
rs1935952 		1.000 0.040 6 108677702 intron variant G/A;C;T snv
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		Mental Disorders 0.010 1.000 1 2011 2011
dbSNP: rs2802292
rs2802292 		0.851 0.160 6 108587315 intron variant G/T snv 0.50
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		Mental Disorders 0.010 1.000 1 2011 2011
dbSNP: rs2802292
rs2802292 		0.851 0.160 6 108587315 intron variant G/T snv 0.50
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs2802292
rs2802292 		0.851 0.160 6 108587315 intron variant G/T snv 0.50
CUI: C3272802
Disease: Hamartomatous polyposis
Hamartomatous polyposis 		Pathological Conditions, Signs and Symptoms; Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs2802292
rs2802292 		0.851 0.160 6 108587315 intron variant G/T snv 0.50
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs4946936
rs4946936 		0.790 0.160 6 108682118 3 prime UTR variant T/A;C snv
CUI: C1847835
Disease: VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding)
VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding) 		Skin and Connective Tissue Diseases 0.010 1.000 1 2014 2014
dbSNP: rs4946936
rs4946936 		0.790 0.160 6 108682118 3 prime UTR variant T/A;C snv
CUI: C0042900
Disease: Vitiligo
Vitiligo 		Skin and Connective Tissue Diseases 0.010 1.000 1 2014 2014
dbSNP: rs4946936
rs4946936 		0.790 0.160 6 108682118 3 prime UTR variant T/A;C snv
CUI: C0023452
Disease: Childhood Acute Lymphoblastic Leukemia
Childhood Acute Lymphoblastic Leukemia 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2014 2014
dbSNP: rs12212067
rs12212067 		0.716 0.320 6 108659993 intron variant T/G snv 0.14
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.030 0.667 3 2013 2015
dbSNP: rs12212067
rs12212067 		0.716 0.320 6 108659993 intron variant T/G snv 0.14
CUI: C2747816
Disease: Complicated malaria
Complicated malaria 		Infections 0.020 0.500 2 2013 2015
dbSNP: rs12212067
rs12212067 		0.716 0.320 6 108659993 intron variant T/G snv 0.14
CUI: C0149696
Disease: Food intolerance (disorder)
Food intolerance (disorder) 		Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2015 2015
dbSNP: rs12212067
rs12212067 		0.716 0.320 6 108659993 intron variant T/G snv 0.14
CUI: C0024535
Disease: Malaria, Falciparum
Malaria, Falciparum 		Infections 0.010 1.000 1 2015 2015
dbSNP: rs3800229
rs3800229 		1.000 0.040 6 108675760 intron variant G/T snv 0.54
CUI: C0562350
Disease: Hip circumference
Hip circumference 		0.700 1.000 1 2015 2015
dbSNP: rs9400239
rs9400239 		1.000 6 108656460 5 prime UTR variant T/C snv 0.55
CUI: C0455829
Disease: Waist Circumference
Waist Circumference 		0.700 1.000 1 2015 2015
dbSNP: rs12212067
rs12212067 		0.716 0.320 6 108659993 intron variant T/G snv 0.14
CUI: C0024530
Disease: Malaria
Malaria 		Infections 0.020 1.000 2 2015 2016
dbSNP: rs12212067
rs12212067 		0.716 0.320 6 108659993 intron variant T/G snv 0.14
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.020 0.500 2 2013 2016
dbSNP: rs12212067
rs12212067 		0.716 0.320 6 108659993 intron variant T/G snv 0.14
CUI: C0041296
Disease: Tuberculosis
Tuberculosis 		Infections 0.010 1.000 1 2016 2016
dbSNP: rs12212067
rs12212067 		0.716 0.320 6 108659993 intron variant T/G snv 0.14
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies 		Cardiovascular Diseases 0.010 1.000 1 2016 2016
dbSNP: rs12212067
rs12212067 		0.716 0.320 6 108659993 intron variant T/G snv 0.14
CUI: C0041234
Disease: Chagas Disease
Chagas Disease 		Infections 0.010 < 0.001 1 2016 2016
dbSNP: rs12212067
rs12212067 		0.716 0.320 6 108659993 intron variant T/G snv 0.14
CUI: C0240094
Disease: Joint tenderness
Joint tenderness 		Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases 0.010 1.000 1 2016 2016
dbSNP: rs12212067
rs12212067 		0.716 0.320 6 108659993 intron variant T/G snv 0.14
CUI: C0679362
Disease: Tuberculosis, extrapulmonary
Tuberculosis, extrapulmonary 		Infections 0.010 1.000 1 2016 2016
dbSNP: rs12212067
rs12212067 		0.716 0.320 6 108659993 intron variant T/G snv 0.14
CUI: C1609538
Disease: Latent Tuberculosis
Latent Tuberculosis 		Infections 0.010 1.000 1 2016 2016
dbSNP: rs12212067
rs12212067 		0.716 0.320 6 108659993 intron variant T/G snv 0.14
CUI: C0151332
Disease: Active tuberculosis
Active tuberculosis 		Infections 0.010 1.000 1 2016 2016
dbSNP: rs12212067
rs12212067 		0.716 0.320 6 108659993 intron variant T/G snv 0.14
CUI: C0041327
Disease: Tuberculosis, Pulmonary
Tuberculosis, Pulmonary 		Infections; Respiratory Tract Diseases 0.010 1.000 1 2016 2016