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	rs3785152 dbSNP Ensembl
Location	Chr16:55716550(Fwd)
Variant Alleles	T/C
Ancestral Allele	C
Functional Annotation	intron_variant.
Consequence to Transcript	intron_variant(ENST00000219833; ENST00000561820; ENST00000568529; ENST00000567238; ENST00000379906; ENST00000568943; ENST00000566163; ENST00000414754)
No. of Studies	2 (significant: 0; non-significant: 2; trend: 0)
Source	Literature-origin

SNP related studies (count: 2)

Reference	Allele Change	Risk Allele	Statistical Values	Author Comments	Result of Statistical Analysis
Sengupta, S. M., 2012	C/T		P-value=0.14, Z statistic (allele 1)=1.46 P-value=0.14, Z statistic (allele 1)=1.46	No significant association was found in this study. No significant association was found in this study.	Non-significant
Kim JW, 2008			X²=3.789, P-value=0.051, OR=1.38 X²=3.789, P-value=0.051, OR=1.38	not associated with ADHD not associated with ADHD	Non-significant

SNP related genes (count: 2)

Literature-origin genes (count: 2)

Approved Symbol	Approved Name	Location	No. of Studies (significant/non-significant/trend)
SLC6A2	solute carrier family 6 (neurotransmitter transporter, noradrenalin), member 2	16q12.2	16(10/5/1)
NET1	neuroepithelial cell transforming 1	10p15	0

Genes from other sources (count: 0)

SNPs in LD with rs3785152 (count: 0) View in gBrowse (chr16:55716550..55716550 )