EMX2, empty spiracles homeobox 2, 2018

N. diseases: 59; N. variants: 2
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1411887961
rs1411887961
Entrez Id: 2018;196047
Gene Symbol: EMX2;EMX2OS
EMX2;EMX2OS
CUI: C0266484
Disease:
Schizencephaly 		T 0.700 CausalMutation CLINVAR
dbSNP: rs1564751655
rs1564751655
Entrez Id: 2018;196047
Gene Symbol: EMX2;EMX2OS
EMX2;EMX2OS
CUI: C0266484
Disease:
Schizencephaly 		A 0.700 CausalMutation CLINVAR