ADHDgene Database

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Large-scale studies

Data Summary

Published Variant
- SNP: 1391
- CNV: 398
- Others: 173
Published Gene: 359
Published Region: 128
Pathway by PBA: 8
Study: 361

Detail ...

SNP Report

Basic Info

Name	rs206936 dbSNP Ensembl
Location	chr6:34302869(Fwd)
Variant Alleles	A/G
Ancestral Allele	G
Functional Annotation	intron_variant.
Consequence to Transcript	intron_variant(ENST00000605528; ENST00000607016)
No. of Studies	1 (significant: 1; non-significant: 0; trend: 0)
Source	Literature-origin

SNP related studies (count: 1)

Reference	Allele Change	Risk Allele	Statistical Values	Author Comments	Result of Statistical Analysis
Albayrak O., 2013			ADHD risk, P-value=3.4E-04, corrected P-value=0.01, OR=1.39;...... ADHD risk, P-value=3.4E-04, corrected P-value=0.01, OR=1.39; Association to ADHD subphenotypes in the German sample, inattention, P-value=0.02, hyperactivity/impulsivity P-value=0.28; Association to ADHD subphenotypes in ADHD meta-analysis data, inattention, P-value=0.09, hyperactivity/impulsivity P-value=0.7, inattention and hyperactivity/impulsivity, P-value=0.54 More...	We detected association with an increased risk for ADHD for ...... We detected association with an increased risk for ADHD for the obesity risk allele G at SNP rs206936. The BMI SNP risk alleles were associated with the quantitative trait inattention with uncorrected P-values below 0.05. More...	Significant

SNP related genes (count: 2)

Literature-origin genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (significant/non-significant/trend)
NUDT3	nudix (nucleoside diphosphate linked moiety X)-type motif 3	6p21.2	1(1/0/0)

Genes from other sources (count: 1)

Approved Symbol	Approved Name	Location
RPS10-NUDT3	RPS10-NUDT3 readthrough	6p21.31

SNPs in LD with rs206936 (count: 32) View in gBrowse (chr6:34255476..34405715 )

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

Literature-origin SNPs (count: 0)

LD-proxies (count: 32)

rs_ID	Functional Annotation	r²[population]
rs6935129	intron_variant	0.815[JPT]
rs414739	intron_variant	1.0[CEU]; 0.954[CHB]; 0.953[JPT]; 0.857[YRI]
rs9366856		1.0[CEU]; 0.826[JPT]
rs6930978	intron_variant	1.0[CEU]; 1.0[TSI]; 0.835[ASW]; 1.0[CHB]; 0.954[CHD]; 0.908[JPT]; 0.807[LWK]; 1.0[MEX]
rs3798562	intron_variant	0.828[CHD]; 0.865[JPT]
rs4711390	intron_variant	0.868[CHD]; 0.865[JPT]
rs16889714	intron_variant; nc_transcript_variant	0.811[JPT]
rs4713770	intron_variant	0.867[CHB]
rs4713776	intron_variant	0.815[JPT]
rs3798564	intron_variant	0.815[JPT]
rs6925243	downstream_gene_variant; intron_variant	0.835[ASW]; 0.907[CHD]; 0.859[JPT]
rs206919	intron_variant	1.0[CEU]; 1.0[TSI]; 0.887[ASW]; 0.954[CHB]; 0.977[CHD]; 0.953[JPT]; 0.807[LWK]; 1.0[MEX]; 0.854[MKK]; 0.858[YRI]
rs206941	intron_variant	1.0[CHB]; 0.908[JPT]; 0.858[YRI]
rs4713777	intron_variant	0.861[CHD]; 0.859[JPT]
rs16889706	downstream_gene_variant; intron_variant	0.86[CHD]; 0.859[JPT]
rs3778077	intron_variant	0.865[JPT]
rs7752035	intron_variant	0.83[CHB]; 0.908[JPT]
rs206921	intron_variant	1.0[CEU]; 1.0[TSI]; 0.887[ASW]; 1.0[CHB]; 0.976[CHD]; 1.0[JPT]; 0.811[LWK]; 0.857[YRI]
rs206942	3_prime_UTR_variant; downstream_gene_variant	0.939[CEU]; 1.0[TSI]; 0.826[ASW]; 1.0[CHB]; 0.93[CHD]; 0.908[JPT]; 0.807[LWK]; 0.869[MEX]; 0.858[YRI]
rs16885998	intron_variant	0.828[CHD]
rs3913009	upstream_gene_variant	1.0[CEU]; 0.826[JPT]
rs3798560	intron_variant	1.0[CEU]; 1.0[TSI]; 0.887[ASW]; 0.954[CHB]; 0.977[CHD]; 0.953[JPT]; 0.807[LWK]; 1.0[MEX]; 0.854[MKK]; 0.858[YRI]
rs6912971	intron_variant	1.0[CEU]; 1.0[TSI]; 1.0[ASW]; 0.954[CHB]; 1.0[CHD]; 0.953[JPT]; 1.0[GIH]; 0.977[LWK]; 1.0[MEX]; 1.0[MKK]; 1.0[YRI]
rs568502	intron_variant	1.0[CEU]; 1.0[CHB]; 0.908[JPT]; 0.887[YRI]
rs9368813		1.0[CEU]; 1.0[TSI]; 0.941[ASW]; 0.829[CHB]; 0.908[CHD]; 0.826[JPT]; 0.955[MEX]; 0.822[MKK]
rs12662905	intron_variant	0.835[ASW]; 0.87[CHB]; 0.977[CHD]; 0.908[JPT]
rs464553	intron_variant	1.0[CEU]; 1.0[TSI]; 1.0[ASW]; 0.954[CHB]; 1.0[CHD]; 0.953[JPT]; 1.0[GIH]; 0.977[LWK]; 1.0[MEX]; 1.0[MKK]; 1.0[YRI]
rs3913010	upstream_gene_variant	0.814[JPT]
rs611928	intron_variant	1.0[CEU]; 1.0[TSI]; 0.887[ASW]; 1.0[CHB]; 0.954[CHD]; 0.908[JPT]; 0.807[LWK]; 1.0[MEX]; 0.858[YRI]
rs4713774	intron_variant	0.865[JPT]
rs9394215		1.0[CEU]
rs6924682	intron_variant	0.83[CHB]; 0.932[CHD]; 0.908[JPT]