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: 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: 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: rs2022464
rs2022464 		6 108624167 intron variant A/C;T snv 0.56
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs4946935
rs4946935 		1.000 0.040 6 108679539 intron variant A/G snv 0.54
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 2 2018 2019
dbSNP: rs2802288
rs2802288 		6 108575012 intron variant A/G snv 0.50
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019
dbSNP: rs3800227
rs3800227 		6 108672958 intron variant A/G snv 0.58
CUI: C0037369
Disease: Smoking
Smoking 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs4946935
rs4946935 		1.000 0.040 6 108679539 intron variant A/G snv 0.54
CUI: C0041296
Disease: Tuberculosis
Tuberculosis 		Infections 0.010 1.000 1 2019 2019
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: 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: rs9486913
rs9486913 		6 108639637 intron variant C/G snv 0.20
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		0.700 1.000 1 2016 2016
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: rs9398171
rs9398171 		1.000 0.040 6 108662324 intron variant C/T snv 0.55
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 3 2015 2019
dbSNP: rs12206094
rs12206094 		6 108584997 intron variant C/T snv 0.31
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2019 2019
dbSNP: rs12206094
rs12206094 		6 108584997 intron variant C/T snv 0.31
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs13217795
rs13217795 		0.925 0.120 6 108652895 intron variant C/T snv 0.55
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2017 2017
dbSNP: rs13217795
rs13217795 		0.925 0.120 6 108652895 intron variant C/T snv 0.55
CUI: C2607914
Disease: Allergic rhinitis (disorder)
Allergic rhinitis (disorder) 		Respiratory Tract Diseases; Immune System Diseases; Otorhinolaryngologic Diseases 0.010 1.000 1 2017 2017