Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
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