ADHDgene Database

SNP Report

Basic Info

Name	rs509360 dbSNP Ensembl
Location	Chr11:61548559(Fwd)
Variant Alleles	A/G
Ancestral Allele	A
Functional Annotation	downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000536352; ENST00000327797) intron_variant(ENST00000278836; ENST00000535042; ENST00000389602; ENST00000537318; ENST00000546247; ENST00000265460) nc_transcript_variant(ENST00000535042; ENST00000537318; ENST00000546247) upstream_gene_variant(ENST00000539361)
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
C11orf9	chromosome 11 open reading frame 9	11q12-q13.1

SNPs in LD with rs509360 (count: 2) View in gBrowse (chr11:61548559..61571348 )

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]

rs174545	3_prime_UTR_variant; downstream_gene_variant; intron_variant	1(0/1/0)	1.0[CHB]; 1.0[JPT]
rs174548	5_prime_UTR_variant; intron_variant; nc_transcript_variant	1(0/1/0)	1.0[CHB]; 0.864[CHD]; 1.0[JPT]