ADHDgene Database

SNP Report

Basic Info

Name	rs6806677 dbSNP Ensembl
Location	Chr3:143058663(Fwd)
Variant Alleles	T/G
Ancestral Allele	T
Functional Annotation	intron_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000316549) upstream_gene_variant(ENST00000479030)
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	No. of Studies (significant/non-significant/trend)
SLC9A9	solute carrier family 9 (sodium/hydrogen exchanger), member 9	3q23-q24	2(2/0/0)

Approved Symbol	Approved Name	Location
SLC9A9-AS1	SLC9A9 antisense RNA 1	3q24

SNPs in LD with rs6806677 (count: 1) View in gBrowse (chr3:143056467..143058663 )

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]

rs7632299	intron_variant; upstream_gene_variant	1(1/0/0)	0.916[CHB]; 0.944[JPT]