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: rs1536057
rs1536057 		1.000 0.040 6 108564420 intron variant C/T snv 0.30
CUI: C3828530
Disease: Platelet Component Distribution Width Measurement
Platelet Component Distribution Width Measurement 		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: 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: 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: 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: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.010 1.000 1 2017 2017
dbSNP: rs2802292
rs2802292 		0.851 0.160 6 108587315 intron variant G/T snv 0.50
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension 		Cardiovascular Diseases 0.010 1.000 1 2016 2016
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: rs13220810
rs13220810 		1.000 0.080 6 108591998 intron variant T/C snv 0.17
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs9480865
rs9480865 		6 108595370 intron variant T/C snv 0.18
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 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: 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: rs3813498
rs3813498 		6 108622962 intron variant C/T snv 0.71
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs3813498
rs3813498 		6 108622962 intron variant C/T snv 0.71
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
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