ADHDgene Database

SNP Report

Basic Info

Name	rs6466484 dbSNP Ensembl
Location	Chr7:114012911(Fwd)
Variant Alleles	A/C
Ancestral Allele	A
Functional Annotation	NMD_transcript_variant; intron_variant; nc_transcript_variant.
Consequence to Transcript	NMD_transcript_variant(ENST00000412402; ENST00000441290; ENST00000440349) intron_variant(ENST00000412402; ENST00000441290; ENST00000440349; ENST00000495516; ENST00000324462; ENST00000393500) nc_transcript_variant(ENST00000495516)
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)
FOXP2	forkhead box P2	7q31	1(1/0/0)

SNPs in LD with rs6466484 (count: 2) View in gBrowse (chr7:114012911..114080435 )

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]

rs10486026	NMD_transcript_variant; intron_variant; nc_transcript_variant	1(0/1/0)	1.0[JPT]
rs10228350	NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant	1(0/1/0)	1.0[CHB]; 1.0[JPT]