ADHDgene Database

SNP Report

Basic Info

Name	rs13087941 dbSNP Ensembl
Location	Chr3:8787220(Fwd)
Variant Alleles	T/C
Ancestral Allele	C
Functional Annotation	downstream_gene_variant; intron_variant; nc_transcript_variant; synonymous_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000316793) intron_variant(ENST00000472766) nc_transcript_variant(ENST00000472766) synonymous_variant(ENST00000343849; ENST00000397368; LRG_329_t1) upstream_gene_variant(ENST00000435138; ENST00000478513)
No. of Studies	0 (significant: 0; non-significant: 0; trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 4)

Approved Symbol	Approved Name	Location	No. of Studies (significant/non-significant/trend)
OXTR	oxytocin receptor	3p25	1(0/1/0)

Approved Symbol	Approved Name	Location
C3orf32	chromosome 3 open reading frame 32	3p25.3
CAV3	caveolin 3	3p25
SSUH2	ssu-2 homolog (C. elegans)	3p26.1

SNPs in LD with rs13087941 (count: 1) View in gBrowse (chr3:8787220..8793724 )

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]

rs6770632	3_prime_UTR_variant; intron_variant; nc_transcript_variant	1(0/1/0)	0.803[CEU]