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	rs6133098 dbSNP Ensembl
Location	Chr20:4217249(Fwd)
Variant Alleles	G/C
Ancestral Allele	G
Functional Annotation	intron_variant.
Consequence to Transcript	intron_variant(ENST00000379453)
No. of Studies	1 (significant: 0; non-significant: 1; trend: 0)
Source	Literature-origin

SNP related studies (count: 1)

Reference	Allele Change	Risk Allele	Statistical Values	Author Comments	Result of Statistical Analysis
Hawi, Z., 2012	G:C	G	P-value=0.887, X²=0.02, OR=1.02, 95% CI=0.77-1.34 P-value=0.887, X²=0.02, OR=1.02, 95% CI=0.77-1.34	The marker did not show significant association with ADHD. The marker did not show significant association with ADHD.	Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources (count: 0)

SNPs in LD with rs6133098 (count: 0) View in gBrowse (chr20:4217249..4217249 )