ADHDgene Database

SNP Report

Basic Info

Name	rs7934165 dbSNP Ensembl
Location	Chr11:27731983(Fwd)
Variant Alleles	G/A
Ancestral Allele	G
Functional Annotation	intron_variant; nc_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000395981; ENST00000395978; ENST00000532997; ENST00000525950; ENST00000314915; ENST00000530663) nc_transcript_variant(ENST00000530663)
No. of Studies	0 (significant: 0; non-significant: 0; trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (significant/non-significant/trend)
BDNF	brain-derived neurotrophic factor	11p14.1	14(8/6/0)

SNPs in LD with rs7934165 (count: 8) View in gBrowse (chr11:27665543..27749725 )

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]

rs11030096	intron_variant; nc_transcript_variant	1(1/0/0)	0.922[CEU]; 0.869[GIH]; 0.912[TSI]
rs11030101	5_prime_UTR_variant; NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant	1(1/0/0)	0.96[CEU]
rs11030104	NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant	2(1/1/0)	0.824[CHD]
rs2049046	downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant	1(0/1/0)	0.959[CEU]; 1.0[CHB]; 1.0[JPT]; 1.0[YRI]
rs6265	3_prime_UTR_variant; NMD_transcript_variant; downstream_gene_variant; intron_variant; missense_variant; nc_transcript_variant; non_coding_exon_variant	12(3/9/0)	0.826[CHD]
rs1491850	intron_variant; nc_transcript_variant	1(1/0/0)	0.801[CHD]
rs7103411	NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant	2(2/0/0)	0.846[CHD]
rs10767664	intron_variant; nc_transcript_variant; upstream_gene_variant	1(1/0/0)	0.855[CHB]