ADHDgene Database

SNP Report

Basic Info

Name	rs1490046 dbSNP Ensembl
Location	Chr5:173956047(Fwd)
Variant Alleles	G/A
Ancestral Allele	G
Functional Annotation	downstream_gene_variant; intron_variant; nc_transcript_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000510234; ENST00000515513; ENST00000504512; ENST00000507361) intron_variant(ENST00000506862) nc_transcript_variant(ENST00000506862)
No. of Studies	1 (significant: 0; non-significant: 0; trend: 1)
Source	Literature-origin

SNP related studies (count: 1)

Reference	Allele Change	Risk Allele	Statistical Values	Author Comments	Result of Statistical Analysis
Stergiakouli E., 2012	A/G	A	P=0.0000287, OR=1.56, 95% CI=1.27-1.92 P=0.0000287, OR=1.56, 95% CI=1.27-1.92	One of the top 35 independent SNP in this ADHD GWAS. One of the top 35 independent SNP in this ADHD GWAS.	Trend

SNP related genes (count: 0)

SNPs in LD with rs1490046 (count: 1) View in gBrowse (chr5:173956047..173959218 )

The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r²>=0.8.