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: rs17069665
rs17069665 		0.882 0.120 6 108620265 intron variant A/C;G snv
CUI: C0242596
Disease: Neoplasm, Residual
Neoplasm, Residual 		Pathological Conditions, Signs and Symptoms; Neoplasms 0.010 1.000 1 2020 2020
dbSNP: rs17069665
rs17069665 		0.882 0.120 6 108620265 intron variant A/C;G snv
CUI: C0023449
Disease: Acute lymphocytic leukemia
Acute lymphocytic leukemia 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2020 2020
dbSNP: rs17069665
rs17069665 		0.882 0.120 6 108620265 intron variant A/C;G snv
CUI: C0751606
Disease: Adult Acute Lymphocytic Leukemia
Adult Acute Lymphocytic Leukemia 		0.010 1.000 1 2020 2020
dbSNP: rs17069665
rs17069665 		0.882 0.120 6 108620265 intron variant A/C;G 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 2020 2020
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: rs2253310
rs2253310 		6 108567390 intron variant C/G;T snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs2490272
rs2490272 		6 108574183 intron variant C/G;T snv
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2017 2017
dbSNP: rs2764261
rs2764261 		6 108606639 intron variant A/G;T snv
CUI: C1314691
Disease: Age at menarche
Age at menarche 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs2764261
rs2764261 		6 108606639 intron variant A/G;T snv
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs2764261
rs2764261 		6 108606639 intron variant A/G;T snv
CUI: C4049938
Disease: Physical Activity Measurement
Physical Activity Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs4946936
rs4946936 		0.790 0.160 6 108682118 3 prime UTR variant T/A;C snv
CUI: C1337013
Disease: Differentiated Thyroid Gland Carcinoma
Differentiated Thyroid Gland Carcinoma 		0.010 1.000 1 2018 2018
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: C0027339
Disease: Nail Diseases
Nail Diseases 		Skin and Connective Tissue Diseases 0.010 1.000 1 2019 2019
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: rs4946936
rs4946936 		0.790 0.160 6 108682118 3 prime UTR variant T/A;C snv
CUI: C0033860
Disease: Psoriasis
Psoriasis 		Skin and Connective Tissue Diseases 0.010 1.000 1 2019 2019
dbSNP: rs4946936
rs4946936 		0.790 0.160 6 108682118 3 prime UTR variant T/A;C snv
CUI: C0278996
Disease: Malignant Head and Neck Neoplasm
Malignant Head and Neck Neoplasm 		Neoplasms 0.010 1.000 1 2019 2019
dbSNP: rs4946936
rs4946936 		0.790 0.160 6 108682118 3 prime UTR variant T/A;C snv
CUI: C3887461
Disease: Head and Neck Carcinoma
Head and Neck Carcinoma 		Neoplasms 0.010 1.000 1 2019 2019
dbSNP: rs9285397
rs9285397 		6 108630452 intron variant T/C;G snv
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs9400241
rs9400241 		0.882 0.120 6 108682786 3 prime UTR variant C/A;G snv
CUI: C0751606
Disease: Adult Acute Lymphocytic Leukemia
Adult Acute Lymphocytic Leukemia 		0.010 1.000 1 2020 2020
dbSNP: rs9400241
rs9400241 		0.882 0.120 6 108682786 3 prime UTR variant C/A;G snv
CUI: C0023449
Disease: Acute lymphocytic leukemia
Acute lymphocytic leukemia 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2020 2020
dbSNP: rs9400241
rs9400241 		0.882 0.120 6 108682786 3 prime UTR variant C/A;G 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 2020 2020
dbSNP: rs9400241
rs9400241 		0.882 0.120 6 108682786 3 prime UTR variant C/A;G snv
CUI: C0242596
Disease: Neoplasm, Residual
Neoplasm, Residual 		Pathological Conditions, Signs and Symptoms; Neoplasms 0.010 1.000 1 2020 2020
dbSNP: rs147856773
rs147856773 		1.000 0.040 6 108666024 intron variant -/GGT delins 0.14
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.700 1.000 1 2017 2017
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