ADHDgene Database

SNP Report

Basic Info

Name	rs9909362 dbSNP Ensembl
Location	Chr17:21215204(Fwd)
Variant Alleles	C/T
Ancestral Allele	C
Functional Annotation	NMD_transcript_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant.
Consequence to Transcript	NMD_transcript_variant(ENST00000496046; ENST00000395491) intron_variant(ENST00000316920; ENST00000342679; ENST00000496046; ENST00000395491; ENST00000361818) nc_transcript_variant(ENST00000477540) non_coding_exon_variant(ENST00000477540) upstream_gene_variant(ENST00000527123)
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)
MAP2K3	mitogen-activated protein kinase kinase 3	17q11.2	1(0/1/0)

SNPs in LD with rs9909362 (count: 1) View in gBrowse (chr17:21193618..21215204 )

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]

rs3760201	NMD_transcript_variant; intron_variant; nc_transcript_variant	1(0/1/0)	0.87[CHB]