ADHDgene Database

SNP Report

Basic Info

Name	rs2175888 dbSNP Ensembl
Location	Chr11:103279597(Fwd)
Variant Alleles	G/A
Ancestral Allele	G
Functional Annotation	NMD_transcript_variant; downstream_gene_variant; intron_variant; upstream_gene_variant.
Consequence to Transcript	NMD_transcript_variant(ENST00000528670) downstream_gene_variant(ENST00000528866) intron_variant(ENST00000375735; ENST00000334267; ENST00000398093; ENST00000533197; ENST00000528670) upstream_gene_variant(ENST00000529569; ENST00000532655; ENST00000528255; ENST00000522384)
No. of Studies	0 (significant: 0; non-significant: 0; trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 3)

Approved Symbol	Approved Name	Location
MTND1P36	MT-ND1 pseudogene 36	11q22.3
MTND2P26	MT-ND2 pseudogene 26	11q22.3
DYNC2H1	dynein, cytoplasmic 2, heavy chain 1	11q21-q22.1

SNPs in LD with rs2175888 (count: 3) View in gBrowse (chr11:103279597..103403862 )

The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r²>=0.8.

rs_ID	#studies(significant/non-significant/trend)	r²[population]

rs10895437	1(0/1/0)	1.0[CEU]
rs1481963	1(0/1/0)	1.0[CEU]
rs7105630	1(0/1/0)	1.0[CEU]