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

SNP Report

Basic Info

Name	rs165599 dbSNP Ensembl
Location	Chr22:19956781(Fwd)
Variant Alleles	G/A
Ancestral Allele	G
Functional Annotation	3_prime_UTR_variant; downstream_gene_variant.
Consequence to Transcript	3_prime_UTR_variant(ENST00000361682; ENST00000449653) downstream_gene_variant(ENST00000480792; ENST00000493893; ENST00000403710; ENST00000406259; ENST00000344269; ENST00000428707; ENST00000207636; ENST00000403184; ENST00000401994; ENST00000406522; ENST00000407537; ENST00000495096; ENST00000406520; ENST00000263207; ENST00000412786)
No. of Studies	2 (significant: 1; non-significant: 1; trend: 0)
Source	Literature-origin

SNP related studies (count: 2)

Reference	Allele Change	Risk Allele	Statistical Values	Author Comments	Result of Statistical Analysis
Michaelovsky E, 2008	A/G		P-value=0.02, X²(1)=5.44 P-value=0.02, X²(1)=5.44	showed significant association with ADHD showed significant association with ADHD	Significant
Turic D, 2005(b)	G/A		allelic TRANSMIT P-value (10,000 simulations)=0.71, X^2<...... allelic TRANSMIT P-value (10,000 simulations)=0.71, X²=0.154 More...	did not show preferential transmission of any allele did not show preferential transmission of any allele	Non-significant

SNP related genes (count: 2)

Literature-origin genes (count: 2)

Approved Symbol	Approved Name	Location	No. of Studies (significant/non-significant/trend)
COMT	catechol-O-methyltransferase	22q11.21	25(5/20/0)
ARVCF	armadillo repeat gene deleted in velocardiofacial syndrome	22q11.21	1(1/0/0)

Genes from other sources (count: 0)

SNPs in LD with rs165599 (count: 0) View in gBrowse (chr22:19956781..19956781 )