RBFOX1, RNA binding fox-1 homolog 1, 54715

N. diseases: 103; N. variants: 76
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4787008
rs4787008
Entrez Id: 54715
Gene Symbol: RBFOX1
RBFOX1
CUI: C0011884
Disease:
Diabetic Retinopathy 		G 0.800 GeneticVariation GWASCAT Genome-wide meta-analysis for severe diabetic retinopathy. 21441570 2011
dbSNP: rs4787008
rs4787008
Entrez Id: 54715
Gene Symbol: RBFOX1
RBFOX1
CUI: C0011884
Disease:
Diabetic Retinopathy 		G 0.800 GeneticVariation GWASDB Genome-wide meta-analysis for severe diabetic retinopathy. 21441570 2011
dbSNP: rs3095508
rs3095508
Entrez Id: 54715
Gene Symbol: RBFOX1
RBFOX1
CUI: C0424574
Disease:
Duration of sleep 		C 0.700 GeneticVariation GWASCAT Genome-wide association study identifies genetic loci for self-reported habitual sleep duration supported by accelerometer-derived estimates. 30846698 2019
dbSNP: rs77684884
rs77684884
Entrez Id: 54715
Gene Symbol: RBFOX1
RBFOX1
CUI: C0424574
Disease:
Duration of sleep 		G 0.700 GeneticVariation GWASCAT Genome-wide analysis of insomnia in 1,331,010 individuals identifies new risk loci and functional pathways. 30804565 2019
dbSNP: rs145873257
rs145873257
Entrez Id: 54715
Gene Symbol: RBFOX1
RBFOX1
CUI: C0376532
Disease:
Epilepsy, Rolandic 		A 0.700 CausalMutation CLINVAR Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy. 29358611 2018
dbSNP: rs372761949
rs372761949
Entrez Id: 54715
Gene Symbol: RBFOX1
RBFOX1
CUI: C0376532
Disease:
Epilepsy, Rolandic 		A 0.700 CausalMutation CLINVAR Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy. 29358611 2018
dbSNP: rs974157467
rs974157467
Entrez Id: 54715
Gene Symbol: RBFOX1
RBFOX1
CUI: C0376532
Disease:
Epilepsy, Rolandic 		A 0.700 CausalMutation CLINVAR Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy. 29358611 2018
dbSNP: rs192917960
rs192917960
Entrez Id: 54715
Gene Symbol: RBFOX1
RBFOX1
CUI: C0017601
Disease:
Glaucoma 		T 0.700 GeneticVariation GWASCAT Genome-wide association and admixture analysis of glaucoma in the Women's Health Initiative. 25027321 2014
dbSNP: rs8057643
rs8057643
Entrez Id: 54715
Gene Symbol: RBFOX1
RBFOX1
CUI: C0017636
Disease:
Glioblastoma 		0.010 GeneticVariation BEFREE In group 2, only one of the 16 SNPs, rs8057643 (located on 16p13.2), was significantly associated with glioblastoma age at diagnosis (nominal P = 0.0017; Bonferroni corrected P = 0.054). 17200355 2007
dbSNP: rs8057643
rs8057643
Entrez Id: 54715
Gene Symbol: RBFOX1
RBFOX1
CUI: C1621958
Disease:
Glioblastoma Multiforme 		0.010 GeneticVariation BEFREE In group 2, only one of the 16 SNPs, rs8057643 (located on 16p13.2), was significantly associated with glioblastoma age at diagnosis (nominal P = 0.0017; Bonferroni corrected P = 0.054). 17200355 2007
dbSNP: rs2343519
rs2343519
Entrez Id: 54715
Gene Symbol: RBFOX1
RBFOX1
CUI: C0018099
Disease:
Gout 		0.700 GeneticVariation GWASCAT Gout and type 2 diabetes have a mutual inter-dependent effect on genetic risk factors and higher incidences. 22179738 2012
dbSNP: rs11645781
rs11645781
Entrez Id: 54715
Gene Symbol: RBFOX1
RBFOX1
CUI: C0018810
Disease:
heart rate 		G 0.800 GeneticVariation GWASDB Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders. 23583979 2013
dbSNP: rs11645781
rs11645781
Entrez Id: 54715
Gene Symbol: RBFOX1
RBFOX1
CUI: C0018810
Disease:
heart rate 		G 0.800 GeneticVariation GWASCAT Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders. 23583979 2013
dbSNP: rs7187960
rs7187960
Entrez Id: 54715
Gene Symbol: RBFOX1
RBFOX1
CUI: C0019163
Disease:
Hepatitis B 		A 0.700 GeneticVariation GWASDB New loci associated with chronic hepatitis B virus infection in Han Chinese. 24162738 2013
dbSNP: rs17648524
rs17648524
Entrez Id: 54715
Gene Symbol: RBFOX1
RBFOX1
CUI: C0020490
Disease:
Hyperopia 		0.700 GeneticVariation GWASCAT Genome-wide meta-analysis of myopia and hyperopia provides evidence for replication of 11 loci. 25233373 2014
dbSNP: rs75638798
rs75638798
Entrez Id: 54715
Gene Symbol: RBFOX1
RBFOX1
CUI: C0338656
Disease:
Impaired cognition 		C 0.700 GeneticVariation GWASCAT Variations in the FRA10AC1 Fragile Site and 15q21 Are Associated with Cerebrospinal Fluid Aβ1-42 Level. 26252872 2015
dbSNP: rs11076962
rs11076962
Entrez Id: 54715
Gene Symbol: RBFOX1
RBFOX1
CUI: C0021704
Disease:
Intelligence 		T 0.700 GeneticVariation GWASCAT Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence. 29942086 2018
dbSNP: rs11077204
rs11077204
Entrez Id: 54715
Gene Symbol: RBFOX1
RBFOX1
CUI: C0021704
Disease:
Intelligence 		C 0.700 GeneticVariation GWASCAT A combined analysis of genetically correlated traits identifies 187 loci and a role for neurogenesis and myelination in intelligence. 29326435 2019
dbSNP: rs11077207
rs11077207
Entrez Id: 54715
Gene Symbol: RBFOX1
RBFOX1
CUI: C0021704
Disease:
Intelligence 		C 0.700 GeneticVariation GWASCAT A combined analysis of genetically correlated traits identifies 187 loci and a role for neurogenesis and myelination in intelligence. 29326435 2019
dbSNP: rs11646221
rs11646221
Entrez Id: 54715
Gene Symbol: RBFOX1
RBFOX1
CUI: C0021704
Disease:
Intelligence 		T 0.700 GeneticVariation GWASCAT Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence. 29942086 2018
dbSNP: rs11865256
rs11865256
Entrez Id: 54715
Gene Symbol: RBFOX1
RBFOX1
CUI: C0021704
Disease:
Intelligence 		T 0.700 GeneticVariation GWASCAT Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function. 29844566 2018
dbSNP: rs12709186
rs12709186
Entrez Id: 54715
Gene Symbol: RBFOX1
RBFOX1
CUI: C0021704
Disease:
Intelligence 		A 0.700 GeneticVariation GWASCAT Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function. 29844566 2018
dbSNP: rs3785238
rs3785238
Entrez Id: 54715
Gene Symbol: RBFOX1
RBFOX1
CUI: C0021704
Disease:
Intelligence 		A 0.700 GeneticVariation GWASCAT A combined analysis of genetically correlated traits identifies 187 loci and a role for neurogenesis and myelination in intelligence. 29326435 2019
dbSNP: rs7186834
rs7186834
Entrez Id: 54715
Gene Symbol: RBFOX1
RBFOX1
CUI: C0021704
Disease:
Intelligence 		T 0.700 GeneticVariation GWASCAT Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function. 29844566 2018
dbSNP: rs9934041
rs9934041
Entrez Id: 54715
Gene Symbol: RBFOX1
RBFOX1
CUI: C0021704
Disease:
Intelligence 		T 0.700 GeneticVariation GWASCAT Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function. 29844566 2018