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: 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: 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: 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: 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: rs3800230
rs3800230 		6 108676925 intron variant T/G snv 0.15
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
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: 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: rs9398173
rs9398173 		6 108679113 intron variant T/C snv 0.55
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
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: rs9480866
rs9480866 		6 108641439 intron variant C/T snv 0.19
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		0.700 1.000 1 2016 2016
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: 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: 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: 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: 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: C0042769
Disease: Virus Diseases
Virus Diseases 		Infections 0.010 1.000 1 2018 2018