ADHDgene Database

SNP Report

Basic Info

Name	rs7132127 dbSNP Ensembl
Location	Chr12:5552076(Fwd)
Variant Alleles	C/G
Ancestral Allele	G
Functional Annotation	intron_variant; nc_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000423158; ENST00000535299; ENST00000543548) nc_transcript_variant(ENST00000535299; ENST00000543548)
No. of Studies	1 (significant: 0; non-significant: 1; trend: 0)
Source	Literature-origin

SNP related studies (count: 1)

Reference	Allele Change	Risk Allele	Statistical Values	Author Comments	Result of Statistical Analysis
Syed Z, 2007	C/G	C		Not significant Not significant	Non-significant

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (significant/non-significant/trend)
NTF3	neurotrophin 3	12p13	3(1/2/0)

SNPs in LD with rs7132127 (count: 4) View in gBrowse (chr12:5552076..5561200 )

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	r²[population]
rs10735050	intron_variant; nc_transcript_variant	0.909[JPT]
rs10774330	intron_variant; nc_transcript_variant	0.909[JPT]
rs10492095	intron_variant; nc_transcript_variant	0.806[CHD]
rs17180851	intron_variant; nc_transcript_variant	0.825[JPT]