FOXO1, forkhead box O1, 2308

N. diseases: 380; N. variants: 16
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4325427
rs4325427
Entrez Id: 2308
Gene Symbol: FOXO1
FOXO1
CUI: C0200637
Disease:
Monocyte count procedure
T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs4325427
rs4325427
Entrez Id: 2308
Gene Symbol: FOXO1
FOXO1
CUI: C0750880
Disease:
Monocyte count result
T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs4943794
rs4943794
Entrez Id: 2308
Gene Symbol: FOXO1
FOXO1
CUI: C1527304
Disease:
Allergic Reaction
C 0.700 GeneticVariation GWASCAT Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology. 29083406 2017
dbSNP: rs71718386
rs71718386
Entrez Id: 2308
Gene Symbol: FOXO1
FOXO1
CUI: C0200638
Disease:
Eosinophil count procedure
C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs7986407
rs7986407
Entrez Id: 2308
Gene Symbol: FOXO1
FOXO1
CUI: C0042133
Disease:
Uterine Fibroids
A 0.700 GeneticVariation GWASCAT Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis. 31649266 2019
dbSNP: rs7986407
rs7986407
Entrez Id: 2308
Gene Symbol: FOXO1
FOXO1
CUI: C2242776
Disease:
Plexiform leiomyoma
A 0.700 GeneticVariation GWASCAT Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis. 31649266 2019
dbSNP: rs7986407
rs7986407
Entrez Id: 2308
Gene Symbol: FOXO1
FOXO1
CUI: C0042133
Disease:
Uterine Fibroids
G 0.700 GeneticVariation GWASCAT Variants associating with uterine leiomyoma highlight genetic background shared by various cancers and hormone-related traits. 30194396 2018
dbSNP: rs7986407
rs7986407
Entrez Id: 2308
Gene Symbol: FOXO1
FOXO1
CUI: C2242776
Disease:
Plexiform leiomyoma
G 0.700 GeneticVariation GWASCAT Variants associating with uterine leiomyoma highlight genetic background shared by various cancers and hormone-related traits. 30194396 2018
dbSNP: rs9532563
rs9532563
Entrez Id: 2308
Gene Symbol: FOXO1
FOXO1
CUI: C0524587
Disease:
Mean Corpuscular Volume (result)
C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs9532563
rs9532563
Entrez Id: 2308
Gene Symbol: FOXO1
FOXO1
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs9549243
rs9549243
Entrez Id: 2308
Gene Symbol: FOXO1
FOXO1
CUI: C0013595
Disease:
Eczema
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs17446614
rs17446614
Entrez Id: 2308
Gene Symbol: FOXO1
FOXO1
CUI: C0011881
Disease:
Diabetic Nephropathy
0.020 GeneticVariation BEFREE FOXO1 gene rs17446614 SNP, and the A-C haplotype of rs17446614 and rs17592236 polymorphisms were risk factors for the development of DN. 30987438 2019
dbSNP: rs17446614
rs17446614
Entrez Id: 2308
Gene Symbol: FOXO1
FOXO1
CUI: C0011881
Disease:
Diabetic Nephropathy
0.020 GeneticVariation BEFREE In conclusion, genetic variant rs10823108 in SIRT1 and variant rs17446614 in FoxO1 may contribute to the risk of DN in T2DM patients. 28860538 2017
dbSNP: rs17446614
rs17446614
Entrez Id: 2308
Gene Symbol: FOXO1
FOXO1
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
0.020 GeneticVariation BEFREE In the German subjects at increased risk for type 2 diabetes, SNPs rs2721068 and rs17446614 were significantly (P = 0.0045 and P = 0.0018, respectively) and SNPs rs17446593 and rs2297627 were nominally (P = 0.0091 and P = 0.0387, respectively) associated with beta-cell dysfunction. rs2721068, rs17446614, and rs2297627 were also nominally associated with impaired glucose tolerance (P = 0.0264, P = 0.0162, and P = 0.0221, respectively). 19141580 2009
dbSNP: rs17446614
rs17446614
Entrez Id: 2308
Gene Symbol: FOXO1
FOXO1
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
0.020 GeneticVariation BEFREE In conclusion, genetic variant rs10823108 in SIRT1 and variant rs17446614 in FoxO1 may contribute to the risk of DN in T2DM patients. 28860538 2017
dbSNP: rs2297627
rs2297627
Entrez Id: 2308
Gene Symbol: FOXO1
FOXO1
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
0.020 GeneticVariation BEFREE An intronic SNP rs2297627 associated with early-onset T2D [OR = 1.34 (1.13-1.58), P = 8.7 × 10(-4)] and T2D onset at any age [OR = 1.19 (1.09-1.30), P = 1 × 10(-4) ]. 26337673 2015
dbSNP: rs2297627
rs2297627
Entrez Id: 2308
Gene Symbol: FOXO1
FOXO1
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
0.020 GeneticVariation BEFREE In the German subjects at increased risk for type 2 diabetes, SNPs rs2721068 and rs17446614 were significantly (P = 0.0045 and P = 0.0018, respectively) and SNPs rs17446593 and rs2297627 were nominally (P = 0.0091 and P = 0.0387, respectively) associated with beta-cell dysfunction. rs2721068, rs17446614, and rs2297627 were also nominally associated with impaired glucose tolerance (P = 0.0264, P = 0.0162, and P = 0.0221, respectively). 19141580 2009
dbSNP: rs10507486
rs10507486
Entrez Id: 2308
Gene Symbol: FOXO1
FOXO1
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
0.010 GeneticVariation BEFREE There were six of 1096 single nucleotide polymorphisms in five genes potentially associated with type 2 diabetes: tachykinin receptor 3 (rs1384401), anaplastic lymphoma receptor tyrosine kinase (rs4319896), calcium channel, voltage-dependent, L type, alpha 1D subunit (rs12487452), FOXO1A (rs10507486 and rs7323267), and v-akt murine thymoma viral oncogene homolog 3 (rs897959). 19346957 2009
dbSNP: rs17446614
rs17446614
Entrez Id: 2308
Gene Symbol: FOXO1
FOXO1
CUI: C0271650
Disease:
Impaired glucose tolerance
0.010 GeneticVariation BEFREE In the German subjects at increased risk for type 2 diabetes, SNPs rs2721068 and rs17446614 were significantly (P = 0.0045 and P = 0.0018, respectively) and SNPs rs17446593 and rs2297627 were nominally (P = 0.0091 and P = 0.0387, respectively) associated with beta-cell dysfunction. rs2721068, rs17446614, and rs2297627 were also nominally associated with impaired glucose tolerance (P = 0.0264, P = 0.0162, and P = 0.0221, respectively). 19141580 2009
dbSNP: rs17446614
rs17446614
Entrez Id: 2308
Gene Symbol: FOXO1
FOXO1
CUI: C0036690
Disease:
Septicemia
0.010 GeneticVariation BEFREE We firstly reported that the rs2721068 and rs17446614 were correlated to genetic predisposition to sepsis. 31492105 2019
dbSNP: rs17446614
rs17446614
Entrez Id: 2308
Gene Symbol: FOXO1
FOXO1
CUI: C0243026
Disease:
Sepsis
0.010 GeneticVariation BEFREE We firstly reported that the rs2721068 and rs17446614 were correlated to genetic predisposition to sepsis. 31492105 2019
dbSNP: rs17592236
rs17592236
Entrez Id: 2308
Gene Symbol: FOXO1
FOXO1
CUI: C2239176
Disease:
Liver carcinoma
0.010 GeneticVariation BEFREE Together, these results indicate that the rs17592236 polymorphism is associated with decreasing of HCC hereditary susceptibility likely through modulating the binding affinity of miR-137 to the 3'UTR in FOXO1 messenger RNA (mRNA). 25739100 2015
dbSNP: rs17592236
rs17592236
Entrez Id: 2308
Gene Symbol: FOXO1
FOXO1
CUI: C0011881
Disease:
Diabetic Nephropathy
0.010 GeneticVariation BEFREE FOXO1 gene rs17446614 SNP, and the A-C haplotype of rs17446614 and rs17592236 polymorphisms were risk factors for the development of DN. 30987438 2019
dbSNP: rs2297626
rs2297626
Entrez Id: 2308
Gene Symbol: FOXO1
FOXO1
CUI: C0038013
Disease:
Ankylosing spondylitis
0.010 GeneticVariation BEFREE In the second stage study, an association analysis of FoxO1/rs2297626</span> was per</span>formed in 210 AAU patients with AS and 630 controls. 25414190 2014
dbSNP: rs2297626
rs2297626
Entrez Id: 2308
Gene Symbol: FOXO1
FOXO1
CUI: C0701807
Disease:
Acute anterior uveitis
0.010 GeneticVariation BEFREE In the second stage study, an association analysis of FoxO1/rs2297626</span> was per</span>formed in 210 AAU patients with AS and 630 controls. 25414190 2014