Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1861973
rs1861973
Entrez Id: 2020
Gene Symbol: EN2
EN2
CUI: C1510586
Disease:
Autism Spectrum Disorders
0.040 GeneticVariation BEFREE Subsequent molecular analysis determined that the EN2 ASD-associated haplotype (rs1861972-rs1861973 A-C) functions as a transcriptional activator to increase gene expression. 24520327 2014
dbSNP: rs1861973
rs1861973
Entrez Id: 2020
Gene Symbol: EN2
EN2
CUI: C1510586
Disease:
Autism Spectrum Disorders
0.040 GeneticVariation BEFREE Previously we demonstrated that an intronic haplotype (rs1861972-rs1861973 A-C) in the homeobox transcription factor ENGRAILED2 (EN2) is significantly associated with ASD. 22180456 2012
dbSNP: rs1861973
rs1861973
Entrez Id: 2020
Gene Symbol: EN2
EN2
CUI: C1510586
Disease:
Autism Spectrum Disorders
0.040 GeneticVariation BEFREE Here, we have investigated the association of five markers [rs3735653 (C/T) in exon 1; rs34808376 (GC/-) and rs6150410 (CGCATCCCC/-) in promoter region; rs1861972 (A/G) and rs1861973 (C/T) in the intron] of the gene with autism and ASD in Indian population using family-based approach. 20050924 2010
dbSNP: rs1861973
rs1861973
Entrez Id: 2020
Gene Symbol: EN2
EN2
CUI: C1510586
Disease:
Autism Spectrum Disorders
0.040 GeneticVariation BEFREE Our previous research involving 167 nuclear families from the Autism Genetic Resource Exchange (AGRE) demonstrated that two intronic SNPs, rs1861972 and rs1861973, in the homeodomain transcription factor gene ENGRAILED 2 (EN2) are significantly associated with autism spectrum disorder (ASD). 16252243 2005