EFL1, elongation factor like GTPase 1, 79631

N. diseases: 73; N. variants: 13
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs111491984
rs111491984
Entrez Id: 79631
Gene Symbol: EFL1
EFL1
CUI: C1314691
Disease:
Age at menarche 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs12439619
rs12439619
Entrez Id: 79631
Gene Symbol: EFL1
EFL1
CUI: C0021704
Disease:
Intelligence 		T 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: rs1972460
rs1972460
Entrez Id: 79631
Gene Symbol: EFL1
EFL1
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: rs2665103
rs2665103
Entrez Id: 79631
Gene Symbol: EFL1
EFL1
CUI: C0021704
Disease:
Intelligence 		T 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: rs28420834
rs28420834
Entrez Id: 79631
Gene Symbol: EFL1
EFL1
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: rs2665103
rs2665103
Entrez Id: 79631
Gene Symbol: EFL1
EFL1
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: rs4778665
rs4778665
Entrez Id: 79631
Gene Symbol: EFL1
EFL1
CUI: C0021704
Disease:
Intelligence 		A 0.700 GeneticVariation GWASCAT Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence. 29942086 2018
dbSNP: rs4778988
rs4778988
Entrez Id: 79631
Gene Symbol: EFL1
EFL1
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: rs8025964
rs8025964
Entrez Id: 79631
Gene Symbol: EFL1
EFL1
CUI: C0021704
Disease:
Intelligence 		A 0.700 GeneticVariation GWASCAT Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence. 29942086 2018
dbSNP: rs2134046
rs2134046
Entrez Id: 79631
Gene Symbol: EFL1
EFL1
CUI: C0021704
Disease:
Intelligence 		0.700 GeneticVariation GWASCAT Large-Scale Cognitive GWAS Meta-Analysis Reveals Tissue-Specific Neural Expression and Potential Nootropic Drug Targets. 29186694 2017
dbSNP: rs867371
rs867371
Entrez Id: 79631
Gene Symbol: EFL1
EFL1
CUI: C0021704
Disease:
Intelligence 		0.700 GeneticVariation GWASCAT Large-Scale Cognitive GWAS Meta-Analysis Reveals Tissue-Specific Neural Expression and Potential Nootropic Drug Targets. 29186694 2017
dbSNP: rs1316615934
rs1316615934
Entrez Id: 79631
Gene Symbol: EFL1
EFL1
CUI: C4693704
Disease:
SHWACHMAN-DIAMOND SYNDROME 2 		T 0.700 CausalMutation CLINVAR
dbSNP: rs1441937959
rs1441937959
Entrez Id: 79631
Gene Symbol: EFL1
EFL1
CUI: C0020438
Disease:
Hypercalciuria 		C 0.700 GeneticVariation CLINVAR
dbSNP: rs1441937959
rs1441937959
Entrez Id: 79631
Gene Symbol: EFL1
EFL1
CUI: C0700635
Disease:
Strudwick syndrome 		C 0.700 GeneticVariation CLINVAR
dbSNP: rs1441937959
rs1441937959
Entrez Id: 79631
Gene Symbol: EFL1
EFL1
CUI: C0030312
Disease:
Pancytopenia 		C 0.700 GeneticVariation CLINVAR
dbSNP: rs1441937959
rs1441937959
Entrez Id: 79631
Gene Symbol: EFL1
EFL1
CUI: C0027092
Disease:
Myopia 		C 0.700 GeneticVariation CLINVAR
dbSNP: rs1441937959
rs1441937959
Entrez Id: 79631
Gene Symbol: EFL1
EFL1
CUI: C4693704
Disease:
SHWACHMAN-DIAMOND SYNDROME 2 		C 0.700 GeneticVariation CLINVAR
dbSNP: rs1441937959
rs1441937959
Entrez Id: 79631
Gene Symbol: EFL1
EFL1
CUI: C4025790
Disease:
Specific learning disability 		C 0.700 GeneticVariation CLINVAR
dbSNP: rs1441937959
rs1441937959
Entrez Id: 79631
Gene Symbol: EFL1
EFL1
CUI: C0235991
Disease:
Small for gestational age (disorder) 		C 0.700 GeneticVariation CLINVAR
dbSNP: rs1441937959
rs1441937959
Entrez Id: 79631
Gene Symbol: EFL1
EFL1
CUI: C0456070
Disease:
Growth delay 		C 0.700 GeneticVariation CLINVAR
dbSNP: rs1441937959
rs1441937959
Entrez Id: 79631
Gene Symbol: EFL1
EFL1
CUI: C0040034
Disease:
Thrombocytopenia 		C 0.700 GeneticVariation CLINVAR
dbSNP: rs1441937959
rs1441937959
Entrez Id: 79631
Gene Symbol: EFL1
EFL1
CUI: C0544755
Disease:
Genu varum 		C 0.700 GeneticVariation CLINVAR
dbSNP: rs1441937959
rs1441937959
Entrez Id: 79631
Gene Symbol: EFL1
EFL1
CUI: C0541764
Disease:
Delayed bone age 		C 0.700 GeneticVariation CLINVAR
dbSNP: rs1441937959
rs1441937959
Entrez Id: 79631
Gene Symbol: EFL1
EFL1
CUI: C0018681
Disease:
Headache 		C 0.700 GeneticVariation CLINVAR
dbSNP: rs1441937959
rs1441937959
Entrez Id: 79631
Gene Symbol: EFL1
EFL1
CUI: C0009806
Disease:
Constipation 		C 0.700 GeneticVariation CLINVAR