ADHDgene Database

SNP Report

Basic Info

Name	rs3027415 dbSNP Ensembl
Location	ChrX:43614441(Fwd)
Variant Alleles	T/C
Ancestral Allele	T
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=0.0041 for genotype analys...... Case-control test: lowest P-value=0.0041 for genotype analysis, P-value=0.00056 for allele analysis in all adult ADHD; lowest P-value=0.031 for genotype analysis, P-value=0.011 for allele analysis in adult combined ADHD; lowest P-value=0.012 for genotype analysis, P-value=0.0055 for allele analysis in adult inattentive ADHD. More...	Still significant associated with adult all ADHD after corre...... Still significant associated with adult all ADHD after correcting for multiple comparisons More...	Significant

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (significant/non-significant/trend)
MAOB	monoamine oxidase B	Xp11.4-p11.3	6(2/4/0)

SNPs in LD with rs3027415 (count: 5) View in gBrowse (chrX:43614441..43678042 )

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

rs_ID	Functional Annotation	r²[population]
rs5905449	downstream_gene_variant; intron_variant	1.0[ASW]; 0.922[CEU]; 1.0[CHB]; 0.827[GIH]; 1.0[MEX]; 0.955[TSI]
rs3027456	intron_variant; nc_transcript_variant	0.894[MEX]
rs2283729	intron_variant; nc_transcript_variant	0.894[MEX]
rs3027450	intron_variant	1.0[ASW]; 0.922[CEU]; 1.0[CHB]; 0.827[GIH]; 1.0[MEX]; 0.955[TSI]
rs10521432	intron_variant	0.893[MEX]