Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1115535
rs1115535
Entrez Id: 10564
Gene Symbol: ARFGEF2
ARFGEF2
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: rs6019535
rs6019535
Entrez Id: 10564
Gene Symbol: ARFGEF2
ARFGEF2
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: rs6019537
rs6019537
Entrez Id: 10564
Gene Symbol: ARFGEF2
ARFGEF2
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: rs1555811929
rs1555811929
Entrez Id: 10564
Gene Symbol: ARFGEF2
ARFGEF2
CUI: C1842563
Disease:
Heterotopia, Periventricular, Autosomal Recessive 		T 0.700 CausalMutation CLINVAR
dbSNP: rs28937880
rs28937880
Entrez Id: 10564
Gene Symbol: ARFGEF2
ARFGEF2
CUI: C1842563
Disease:
Heterotopia, Periventricular, Autosomal Recessive 		0.700 GeneticVariation UNIPROT
dbSNP: rs398122523
rs398122523
Entrez Id: 10564
Gene Symbol: ARFGEF2
ARFGEF2
CUI: C1842563
Disease:
Heterotopia, Periventricular, Autosomal Recessive 		A 0.700 CausalMutation CLINVAR
dbSNP: rs730882200
rs730882200
Entrez Id: 10564
Gene Symbol: ARFGEF2
ARFGEF2
CUI: C0020255
Disease:
Hydrocephalus 		TC 0.700 GeneticVariation CLINVAR
dbSNP: rs730882200
rs730882200
Entrez Id: 10564
Gene Symbol: ARFGEF2
ARFGEF2
CUI: C0557874
Disease:
Global developmental delay 		TC 0.700 GeneticVariation CLINVAR
dbSNP: rs730882200
rs730882200
Entrez Id: 10564
Gene Symbol: ARFGEF2
ARFGEF2
CUI: C0014544
Disease:
Epilepsy 		TC 0.700 GeneticVariation CLINVAR