ADHDgene Database

SNP Report

Basic Info

Name	rs9534495 dbSNP Ensembl
Location	Chr13:47429228(Fwd)
Variant Alleles	A/G
Ancestral Allele	A
Functional Annotation	downstream_gene_variant; intron_variant; nc_transcript_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000452352) intron_variant(ENST00000455126; ENST00000430913; ENST00000542664; ENST00000543956; ENST00000378688) nc_transcript_variant(ENST00000455126; ENST00000430913)
No. of Studies	1 (significant: 1; non-significant: 0; trend: 0)
Source	Literature-origin

SNP related studies (count: 1)

Reference	Allele Change	Risk Allele	Statistical Values	Author Comments	Result of Statistical Analysis
Ribases M, 2009(b)			Case-control test: lowest P-value=0.042 for genotype analysi...... Case-control test: lowest P-value=0.042 for genotype analysis, P-value=0.043 for allele analysis in all adult ADHD; lowest P-value=0.0079 for genotype analysis, P-value=0.0054 for allele analysis in adult combined ADHD. More...	no significance after correcting for multiple comparisons no significance after correcting for multiple comparisons	Significant

SNP related genes (count: 2)

Approved Symbol	Approved Name	Location	No. of Studies (significant/non-significant/trend)
HTR2A	5-hydroxytryptamine (serotonin) receptor 2A	13q14-q21	12(6/6/0)

Approved Symbol	Approved Name	Location
HTR2A-AS1	HTR2A antisense RNA 1 (non-protein coding)	13q14.2

SNPs in LD with rs9534495 (count: 1) View in gBrowse (chr13:47428471..47429228 )

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