ADHDgene Database

SNP Report

Basic Info

Name	rs4076427 dbSNP Ensembl
Location	Chr17:79087537(Fwd)
Variant Alleles	G/C
Ancestral Allele	G
Functional Annotation	downstream_gene_variant; intron_variant; nc_transcript_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000321280; ENST00000572329; ENST00000575712; ENST00000374792; ENST00000416299; ENST00000575841; ENST00000570932; ENST00000573469; ENST00000576995; ENST00000326724; ENST00000417379) intron_variant(ENST00000428708; ENST00000575245; ENST00000435091; ENST00000576225; ENST00000392411; ENST00000572498; ENST00000321300) nc_transcript_variant(ENST00000576225)
No. of Studies	0 (significant: 0; non-significant: 0; trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

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
AATK	apoptosis-associated tyrosine kinase	17q25.3

SNPs in LD with rs4076427 (count: 2) View in gBrowse (chr17:79056453..79087537 )

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	#studies(significant/non-significant/trend)	r²[population]

rs4075482	NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant	1(0/1/0)	0.924[CEU]; 0.956[CHB]; 1.0[JPT]
rs4969245	NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant	1(0/1/0)	0.954[CHB]; 0.908[JPT]