ADHDgene Database

SNP Report

Basic Info

Name	rs6278 dbSNP Ensembl
Location	Chr11:113280724(Fwd)
Variant Alleles	C/A
Ancestral Allele	C
Functional Annotation	3_prime_UTR_variant; downstream_gene_variant; intron_variant; nc_transcript_variant.
Consequence to Transcript	3_prime_UTR_variant(ENST00000346454; ENST00000362072; ENST00000355319; ENST00000544518; ENST00000542968) downstream_gene_variant(ENST00000538967; ENST00000540600; ENST00000535984) intron_variant(ENST00000546284) nc_transcript_variant(ENST00000546284)
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)
DRD2	dopamine receptor D2	11q22-q23	10(3/7/0)

SNPs in LD with rs6278 (count: 6) View in gBrowse (chr11:113270828..113289182 )

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]

rs1124491	downstream_gene_variant; intron_variant; nc_transcript_variant	1(1/0/0)	1.0[CEU]; 1.0[CHB]; 1.0[JPT]; 1.0[YRI]
rs6279	3_prime_UTR_variant; downstream_gene_variant; intron_variant; nc_transcript_variant	1(0/1/0)	0.83[CHB]
rs1800497	downstream_gene_variant; missense_variant	2(2/0/0)	1.0[CHB]; 1.0[CHD]; 0.836[GIH]; 0.908[JPT]
rs6275	downstream_gene_variant; synonymous_variant	2(0/2/0)	0.909[CHD]
rs1079727	intron_variant; nc_transcript_variant; upstream_gene_variant	1(1/0/0)	1.0[CEU]; 0.955[CHB]; 0.824[CHD]; 0.909[GIH]; 0.858[JPT]; 1.0[MEX]; 1.0[TSI]
rs1079595	downstream_gene_variant; intron_variant; nc_transcript_variant	1(1/0/0)	1.0[CEU]; 1.0[CHB]; 1.0[JPT]