ADHDgene Database

SNP Report

Basic Info

Name	rs10994336 dbSNP Ensembl
Location	Chr10:62179812(Fwd)
Variant Alleles	C/T
Ancestral Allele	C
Functional Annotation	NMD_transcript_variant; intron_variant.
Consequence to Transcript	NMD_transcript_variant(ENST00000510495) intron_variant(ENST00000373827; ENST00000503366; ENST00000510495)
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
Landaas ET, 2011		T	P-value=0.57, OR=0.91 for frequencies of the BD risk alleles...... P-value=0.57, OR=0.91 for frequencies of the BD risk alleles and genotypes in ADHD More...	did not show any association with ADHD did not show any association with ADHD	Non-significant

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (significant/non-significant/trend)
ANK3	ankyrin 3, node of Ranvier (ankyrin G)	10q21	1(0/1/0)

SNPs in LD with rs10994336 (count: 4) View in gBrowse (chr10:62179812..62279124 )

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]
rs10994359	NMD_transcript_variant; intron_variant	0.825[CEU]
rs10994338	NMD_transcript_variant; intron_variant	1.0[CEU]; 1.0[CHB]; 1.0[JPT]
rs4948418	NMD_transcript_variant; intron_variant	0.825[CEU]; 1.0[CHB]; 1.0[JPT]
rs10994397	NMD_transcript_variant; intron_variant; nc_transcript_variant	0.825[CEU]