FOXO1, forkhead box O1, 2308

N. diseases: 380; N. variants: 16
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: rs7986407
rs7986407 		0.882 0.120 13 40605661 intron variant A/G snv 0.38
CUI: C2242776
Disease: Plexiform leiomyoma
Plexiform leiomyoma 		0.700 1.000 2 2018 2019
dbSNP: rs7986407
rs7986407 		0.882 0.120 13 40605661 intron variant A/G snv 0.38
CUI: C0042133
Disease: Uterine Fibroids
Uterine Fibroids 		Neoplasms 0.700 1.000 2 2018 2019
dbSNP: rs4325427
rs4325427 		13 40642397 intron variant C/A;T snv
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs4325427
rs4325427 		13 40642397 intron variant C/A;T snv
CUI: C0750880
Disease: Monocyte count result
Monocyte count result 		0.700 1.000 1 2016 2016
dbSNP: rs4943794
rs4943794 		13 40599271 intron variant G/A;C snv
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		Immune System Diseases 0.700 1.000 1 2017 2017
dbSNP: rs71718386
rs71718386 		13 40650151 intron variant TATA/- delins 0.41
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs9532563
rs9532563 		13 40586133 intron variant T/C snv 0.20
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2016 2016
dbSNP: rs9532563
rs9532563 		13 40586133 intron variant T/C snv 0.20
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2019 2019
dbSNP: rs9549243
rs9549243 		1.000 0.040 13 40643068 intron variant G/A snv 0.21
CUI: C0013595
Disease: Eczema
Eczema 		Skin and Connective Tissue Diseases 0.700 1.000 1 2019 2019
dbSNP: rs17446614
rs17446614 		0.851 0.240 13 40565740 intron variant G/A snv 0.16
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.020 1.000 2 2009 2017
dbSNP: rs17446614
rs17446614 		0.851 0.240 13 40565740 intron variant G/A snv 0.16
CUI: C0011881
Disease: Diabetic Nephropathy
Diabetic Nephropathy 		Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases 0.020 1.000 2 2017 2019
dbSNP: rs2297627
rs2297627 		0.925 0.120 13 40659794 intron variant A/G snv 0.41
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.020 1.000 2 2009 2015
dbSNP: rs10507486
rs10507486 		1.000 0.080 13 40612364 intron variant G/A 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 2009 2009
dbSNP: rs17446614
rs17446614 		0.851 0.240 13 40565740 intron variant G/A snv 0.16
CUI: C0271650
Disease: Impaired glucose tolerance
Impaired glucose tolerance 		Nutritional and Metabolic Diseases 0.010 1.000 1 2009 2009
dbSNP: rs17446614
rs17446614 		0.851 0.240 13 40565740 intron variant G/A snv 0.16
CUI: C0036690
Disease: Septicemia
Septicemia 		Pathological Conditions, Signs and Symptoms; Infections 0.010 1.000 1 2019 2019
dbSNP: rs17446614
rs17446614 		0.851 0.240 13 40565740 intron variant G/A snv 0.16
CUI: C0243026
Disease: Sepsis
Sepsis 		Pathological Conditions, Signs and Symptoms; Infections 0.010 1.000 1 2019 2019
dbSNP: rs17592236
rs17592236 		0.925 0.200 13 40557795 3 prime UTR variant C/T snv 3.7E-02
CUI: C0011881
Disease: Diabetic Nephropathy
Diabetic Nephropathy 		Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs17592236
rs17592236 		0.925 0.200 13 40557795 3 prime UTR variant C/T snv 3.7E-02
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2015 2015
dbSNP: rs2297626
rs2297626 		0.925 0.080 13 40659865 intron variant T/C snv 0.12
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		Musculoskeletal Diseases 0.010 1.000 1 2014 2014
dbSNP: rs2297626
rs2297626 		0.925 0.080 13 40659865 intron variant T/C snv 0.12
CUI: C0701807
Disease: Acute anterior uveitis
Acute anterior uveitis 		Eye Diseases 0.010 1.000 1 2014 2014
dbSNP: rs2297627
rs2297627 		0.925 0.120 13 40659794 intron variant A/G snv 0.41
CUI: C0271650
Disease: Impaired glucose tolerance
Impaired glucose tolerance 		Nutritional and Metabolic Diseases 0.010 1.000 1 2009 2009
dbSNP: rs2297627
rs2297627 		0.925 0.120 13 40659794 intron variant A/G snv 0.41
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.010 1.000 1 2019 2019
dbSNP: rs2721068
rs2721068 		0.882 0.160 13 40565575 intron variant T/C snv 0.38
CUI: C0243026
Disease: Sepsis
Sepsis 		Pathological Conditions, Signs and Symptoms; Infections 0.010 1.000 1 2019 2019
dbSNP: rs2721068
rs2721068 		0.882 0.160 13 40565575 intron variant T/C snv 0.38
CUI: C0036690
Disease: Septicemia
Septicemia 		Pathological Conditions, Signs and Symptoms; Infections 0.010 1.000 1 2019 2019
dbSNP: rs2721068
rs2721068 		0.882 0.160 13 40565575 intron variant T/C snv 0.38
CUI: C0271650
Disease: Impaired glucose tolerance
Impaired glucose tolerance 		Nutritional and Metabolic Diseases 0.010 1.000 1 2009 2009