EN2, engrailed homeobox 2, 2020

N. diseases: 41; N. variants: 8
Disease: Autistic Disorder ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3824068
rs3824068
Entrez Id: 2020
Gene Symbol: EN2
EN2
CUI: C0004352
Disease:
Autistic Disorder 		0.010 GeneticVariation BEFREE However, when haplotypes were constructed with multiple markers, a number of haplotypes including three two-marker haplotypes, nine three-marker haplotypes, one four-marker haplotype, and one six-marker haplotype, all of which contain the major allele A of rs3824068, displayed significantly associated with autism. 17948901 2008