ADHDgene Database

SNP Report

Basic Info

Name	rs7989807 dbSNP Ensembl
Location	Chr13:36625089(Fwd)
Variant Alleles	C/T
Ancestral Allele	C
Functional Annotation	intron_variant.
Consequence to Transcript	intron_variant(ENST00000360631; ENST00000255448; ENST00000379892)
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
Havik, B., 2012			P-value=0.098, OR (95% CI)=1.24 (0.96-1.61) in the Norwegian...... P-value=0.098, OR (95% CI)=1.24 (0.96-1.61) in the Norwegian sample; P-value=0.085, OR (95% CI)=1.22 (0.97-1.53) in the German sample; P-value=0.016, OR (95% CI)=1.29 (1.09-1.53) in the merged sample More...	The marker showed significant association with ADHD. The marker showed significant association with ADHD.	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 rs7989807 (count: 6) View in gBrowse (chr13:36597840..36681361 )

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