ADHDgene Database

SNP Report

Basic Info

Name	rs10835196 dbSNP Ensembl
Location	Chr11:27601335(Fwd)
Variant Alleles	G/C
Ancestral Allele	G
Functional Annotation	intron_variant; nc_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000501176; ENST00000502161; ENST00000499008; ENST00000499568; ENST00000532965; ENST00000530686; ENST00000500662) nc_transcript_variant(ENST00000501176; ENST00000502161; ENST00000499008; ENST00000499568; ENST00000532965; ENST00000530686; ENST00000500662) upstream_gene_variant(ENST00000540179; ENST00000476147)
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
RPS25P1	ribosomal protein S25 pseudogene 1	11p14.1
BDNF-AS1	BDNF antisense RNA 1 (non-protein coding)	11p14.1

SNPs in LD with rs10835196 (count: 2) View in gBrowse (chr11:27528987..27665543 )

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)	0.821[CEU]
rs3763965	intron_variant; nc_transcript_variant; upstream_gene_variant	1(0/1/0)	1.0[CHB]; 1.0[JPT]; 0.83[YRI]