ADHDgene Database

SNP Report

Basic Info

Name	rs3736025 dbSNP Ensembl
Location	Chr8:23112662(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(ENST00000517325; ENST00000519414; ENST00000519503) intron_variant(ENST00000517325; ENST00000519414; ENST00000397677; ENST00000313219; ENST00000519503; ENST00000519529; ENST00000519984) nc_transcript_variant(ENST00000523091; ENST00000519529) non_coding_exon_variant(ENST00000523091) upstream_gene_variant(ENST00000520102; ENST00000521656)
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)
CHMP7	CHMP family, member 7	8p21.2	1(0/0/1)

SNPs in LD with rs3736025 (count: 1) View in gBrowse (chr8:23106665..23112662 )

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]

rs2280934	NMD_transcript_variant; intron_variant; nc_transcript_variant	1(0/0/1)	0.886[GIH]