ADHDgene Database

SNP Report

Basic Info

Name	rs7816032 dbSNP Ensembl
Location	Chr8:19786891(Fwd)
Variant Alleles	C/T
Ancestral Allele	T
Functional Annotation	intron_variant.
Consequence to Transcript	intron_variant(ENST00000520959)
No. of Studies	1 (significant: 0; non-significant: 0; trend: 1)
Source	Literature-origin

SNP related studies (count: 1)

Reference	Allele Change	Risk Allele	Statistical Values	Author Comments	Result of Statistical Analysis
Lasky-Su J, 2008			P-value=2.25E-06 under Recessive model for HI symptom count P-value=2.25E-06 under Recessive model for HI symptom count	association finding with P-value association finding with P-value	Trend

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (significant/non-significant/trend)
LPL	lipoprotein lipase	8p22	1(0/0/1)

SNPs in LD with rs7816032 (count: 6) View in gBrowse (chr8:19774890..19803093 )

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]
rs4466415	intron_variant	1.0[CHB]; 0.915[JPT]
rs28834434	intron_variant	0.85[CEU]; 1.0[CHB]; 0.915[JPT]; 0.854[YRI]
rs1534649	NMD_transcript_variant; intron_variant; nc_transcript_variant	0.812[CHB]; 0.915[JPT]
rs3779788	NMD_transcript_variant; intron_variant; nc_transcript_variant	0.815[CHB]; 1.0[JPT]
rs3779787	NMD_transcript_variant; intron_variant; nc_transcript_variant	1.0[JPT]
rs10104051	NMD_transcript_variant; intron_variant; nc_transcript_variant	0.814[CHB]; 0.915[JPT]