ADHDgene Database

SNP Report

Basic Info

Name	rs7616236 dbSNP Ensembl
Location	Chr3:39542136(Fwd)
Variant Alleles	G/A
Ancestral Allele	G
Functional Annotation	NMD_transcript_variant; intron_variant; upstream_gene_variant.
Consequence to Transcript	NMD_transcript_variant(ENST00000452959) intron_variant(ENST00000447324; ENST00000415443; ENST00000441980; ENST00000436143; ENST00000354668; ENST00000383754; ENST00000451925; ENST00000311042; ENST00000420739; ENST00000452959; ENST00000396228; ENST00000428261) upstream_gene_variant(ENST00000479860; ENST00000442631; ENST00000424090)
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)
MOBP	myelin-associated oligodendrocyte basic protein	3p21.33	1(0/0/1)

SNPs in LD with rs7616236 (count: 1) View in gBrowse (chr3:39542136..39555580 )

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]

rs864643	3_prime_UTR_variant; NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant	1(0/0/1)	0.878[CEU]