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	rs2397771 dbSNP Ensembl
Location	Chr16:55689087(Fwd)
Variant Alleles	C/G
Ancestral Allele	C
Functional Annotation	upstream_gene_variant.
Consequence to Transcript	upstream_gene_variant(ENST00000566163; ENST00000219833; ENST00000561820; ENST00000414754; ENST00000568943; ENST00000568529; ENST00000568655; ENST00000379906)
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
Hawi, Z., 2012	G:C	C	P-value=0.7815, X²=0.08, OR=1.04, 95% CI=0.79-1.3...... P-value=0.7815, X²=0.08, OR=1.04, 95% CI=0.79-1.36 More...	The marker did not show significant association with ADHD. The marker did not show significant association with ADHD.	Non-significant
Sengupta, S. M., 2012	G/C		P-value=0.06, Z statistic (allele 1)=1.85 P-value=0.06, Z statistic (allele 1)=1.85	No significant association was found in this study. No significant association was found in this study.	Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources (count: 0)

SNPs in LD with rs2397771 (count: 0) View in gBrowse (chr16:55689087..55689087 )