ADHDgene Database

SNP Report

Basic Info

Name	rs7327771 dbSNP Ensembl
Location	Chr13:36679512(Fwd)
Variant Alleles	G/A
Ancestral Allele	G
Functional Annotation	intron_variant.
Consequence to Transcript	intron_variant(ENST00000379892; ENST00000360631; ENST00000255448)
No. of Studies	1 (significant: 0; non-significant: 1; trend: 0)
Source	Literature-origin

SNP related studies (count: 1)

Reference	Allele Change	Risk Allele	Statistical Values	Author Comments	Result of Statistical Analysis
Havik, B., 2012			P-value=0.497, OR (95% CI)=1.13 (0.80-1.60) in the Norwegian...... P-value=0.497, OR (95% CI)=1.13 (0.80-1.60) in the Norwegian sample; P-value=0.201, OR (95% CI)=1.19 (0.88-1.62) in the German sample; P-value=0.165, OR (95% CI)=1.21 (0.97-1.52) in the merged sample More...	The marker did not show significant association with ADHD. The marker did not show significant association with ADHD.	Non-significant

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (significant/non-significant/trend)
DCLK1	doublecortin-like kinase 1	13q13.3	1(1/0/0)

SNPs in LD with rs7327771 (count: 3) View in gBrowse (chr13:36674859..36679512 )

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