ADHDgene Database

SNP Report

Basic Info

Name	rs2995300 dbSNP Ensembl
Location	Chr10:135076523(Fwd)
Variant Alleles	C/A
Ancestral Allele	C
Functional Annotation	3_prime_UTR_variant; nc_transcript_variant; non_coding_exon_variant.
Consequence to Transcript	3_prime_UTR_variant(ENST00000445355; ENST00000485491; ENST00000415217) nc_transcript_variant(ENST00000559018) non_coding_exon_variant(ENST00000559018)
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
ADAM8	ADAM metallopeptidase domain 8	10q26.3

SNPs in LD with rs2995300 (count: 2) View in gBrowse (chr10:135076523..135146714 )

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]

rs11101694	intron_variant	1(0/1/0)	0.842[GIH]
rs2275723	3_prime_UTR_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant	1(1/0/0)	0.835[GIH]; 0.808[TSI]