ADHDgene Database

SNP Report

Basic Info

Name	rs4969349 dbSNP Ensembl
Location	Chr17:79006033(Fwd)
Variant Alleles	G/A
Ancestral Allele	G
Functional Annotation	nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant.
Consequence to Transcript	nc_transcript_variant(ENST00000577066; ENST00000573167) non_coding_exon_variant(ENST00000577066; ENST00000573167) upstream_gene_variant(ENST00000572329; ENST00000575750; ENST00000428708; ENST00000575712; ENST00000542745; ENST00000321280; ENST00000570913; ENST00000575989; ENST00000576470; ENST00000321300; ENST00000435091; ENST00000575245; ENST00000392411; ENST00000571530; ENST00000573894)
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
Ribases M, 2009(a)			Case-control test: P-value=0.26 for genotype analysis, P-val...... Case-control test: P-value=0.26 for genotype analysis, P-value=0.89 for allele analysis in Spanish adult ADHD group; P-value=0.69 for genotype analysis, P-value=0.58 for allele analysis in Spanish childhood ADHD group; P-value=0.51 for genotype analysis, P-value=0.46 for allele analysis in German adult ADHD group; P-value=0.75 for genotype analysis, P-value=0.53 for allele analysis in Norwegian adult ADHD group. More...	No association was found. No association was found.	Non-significant

SNP related genes (count: 2)

Approved Symbol	Approved Name	Location	No. of Studies (significant/non-significant/trend)
BAIAP2	BAI1-associated protein 2	17q25	1(1/0/0)

Approved Symbol	Approved Name	Location
BAIAP2-AS1	BAIAP2 antisense RNA 1 (head to head) [VALIDATED Refseq, miscRNA]	17q25.3

SNPs in LD with rs4969349 (count: 1) View in gBrowse (chr17:79004616..79006033 )

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