ADHDgene Database

SNP Report

Basic Info

Name	rs10938813 dbSNP Ensembl
Location	Chr11:115899782(Fwd); Chr11:133365486(Rev); Chr13:51323762(Rev); Chr17:78690055(Rev); Chr4:10799734(Fwd); Chr7:102445452(Fwd)
Variant Alleles	G/A
Functional Annotation	NMD_transcript_variant; intron_variant; nc_transcript_variant.
Consequence to Transcript	NMD_transcript_variant(ENST00000420217; ENST00000442873; ENST00000574767) intron_variant(ENST00000524381; ENST00000529038; ENST00000420217; ENST00000413034; ENST00000409231; ENST00000442873; ENST00000574767; ENST00000570891; ENST00000306801; ENST00000577161; ENST00000544334; ENST00000537330; ENST00000572733; ENST00000400393) nc_transcript_variant(ENST00000529038; ENST00000577161; ENST00000572733)
No. of Studies	0 (significant: 0; non-significant: 0; trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 4)

Approved Symbol	Approved Name	Location
OPCML	opioid binding protein/cell adhesion molecule-like	11q25
DLEU7	deleted in lymphocytic leukemia, 7	13q14.3
RPTOR	regulatory associated protein of MTOR, complex 1	17q25.3
FAM185A	family with sequence similarity 185, member A	7q22.1

SNPs in LD with rs10938813 (count: 1) View in gBrowse (chr11; 11; 13; 17; 4; 7:20851050..115899782 )

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]

rs4697192	NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant	1(1/0/0)	0.95[CHB]; 0.896[JPT]