RBFOX3, RNA binding fox-1 homolog 3, 146713

N. diseases: 30; N. variants: 14
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12949587
rs12949587
Entrez Id: 146713
Gene Symbol: RBFOX3
RBFOX3
CUI: C4721579
Disease:
Secondary malignant neoplasm of colon and/or rectum
0.700 GeneticVariation GWASCAT A genome-wide association study identifies single nucleotide polymorphisms associated with time-to-metastasis in colorectal cancer. 30738427 2019
dbSNP: rs143203352
rs143203352
Entrez Id: 146713
Gene Symbol: RBFOX3
RBFOX3
CUI: C0523829
Disease:
Phosphatidylcholine measurement
C 0.700 GeneticVariation GWASCAT Genetic architecture of human plasma lipidome and its link to cardiovascular disease. 31551469 2019
dbSNP: rs972548690
rs972548690
Entrez Id: 146713
Gene Symbol: RBFOX3
RBFOX3
CUI: C0376532
Disease:
Epilepsy, Rolandic
T 0.700 CausalMutation CLINVAR Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy. 29358611 2018
dbSNP: rs11650709
rs11650709
Entrez Id: 146713
Gene Symbol: RBFOX3
RBFOX3
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
T 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs16972228
rs16972228
Entrez Id: 146713
Gene Symbol: RBFOX3
RBFOX3
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
T 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs2061538
rs2061538
Entrez Id: 146713
Gene Symbol: RBFOX3
RBFOX3
CUI: C3893645
Disease:
response to ACE inhibitor
G 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies on the intolerance of angiotensin-converting enzyme inhibitors. 28030426 2017
dbSNP: rs2377392
rs2377392
Entrez Id: 146713
Gene Symbol: RBFOX3
RBFOX3
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
G 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs2889620
rs2889620
Entrez Id: 146713
Gene Symbol: RBFOX3
RBFOX3
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
C 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs4239026
rs4239026
Entrez Id: 146713
Gene Symbol: RBFOX3
RBFOX3
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
C 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs35570576
rs35570576
Entrez Id: 146713
Gene Symbol: RBFOX3
RBFOX3
CUI: C1863416
Disease:
Autosomal dominant compelling helio ophthalmic outburst syndrome
0.700 GeneticVariation GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965 2016
dbSNP: rs7211029
rs7211029
Entrez Id: 146713
Gene Symbol: RBFOX3
RBFOX3
CUI: C4505222
Disease:
Sleep Onset Latency
0.700 GeneticVariation GWASCAT We found a cluster of three highly correlated variants (rs9900428, rs9907432 and rs7211029) in the RNA-binding protein fox-1 homolog 3 gene (RBFOX3) associated with sleep latency (P-values=5.77 × 10(-08), 6.59 × 10(-)(08) and 9.17 × 10(-)(08)). 27142678 2016
dbSNP: rs1000791
rs1000791
Entrez Id: 146713
Gene Symbol: RBFOX3
RBFOX3
CUI: C0202239
Disease:
Uric acid measurement (procedure)
T 0.700 GeneticVariation GWASCAT Modulation of genetic associations with serum urate levels by body-mass-index in humans. 25811787 2015
dbSNP: rs79211555
rs79211555
Entrez Id: 146713
Gene Symbol: RBFOX3
RBFOX3
CUI: C1519383
Disease:
Smoking Behaviors
0.700 GeneticVariation GWASCAT Mercapturic Acids Derived from the Toxicants Acrolein and Crotonaldehyde in the Urine of Cigarette Smokers from Five Ethnic Groups with Differing Risks for Lung Cancer. 26053186 2015
dbSNP: rs79211555
rs79211555
Entrez Id: 146713
Gene Symbol: RBFOX3
RBFOX3
CUI: C0037369
Disease:
Smoking
0.700 GeneticVariation GWASCAT Mercapturic Acids Derived from the Toxicants Acrolein and Crotonaldehyde in the Urine of Cigarette Smokers from Five Ethnic Groups with Differing Risks for Lung Cancer. 26053186 2015
dbSNP: rs898534
rs898534
Entrez Id: 146713
Gene Symbol: RBFOX3
RBFOX3
CUI: C1305855
Disease:
Body mass index
G 0.700 GeneticVariation GWASCAT Modulation of genetic associations with serum urate levels by body-mass-index in humans. 25811787 2015
dbSNP: rs898534
rs898534
Entrez Id: 146713
Gene Symbol: RBFOX3
RBFOX3
CUI: C0202239
Disease:
Uric acid measurement (procedure)
G 0.700 GeneticVariation GWASCAT Modulation of genetic associations with serum urate levels by body-mass-index in humans. 25811787 2015