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	rs4998 dbSNP Ensembl
Location	chr8:37821486(Fwd)
Variant Alleles	C/G
Ancestral Allele	G
Functional Annotation	3_prime_UTR_variant; nc_transcript_variant; non_coding_exon_variant.
Consequence to Transcript	3_prime_UTR_variant(ENST00000345060) nc_transcript_variant(ENST00000520341) non_coding_exon_variant(ENST00000520341)
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	C	P-value=0.9013, X²=0.02, OR=1.03, 95% CI=0.63-1.6...... P-value=0.9013, X²=0.02, OR=1.03, 95% CI=0.63-1.67 More...	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 rs4998 (count: 0) View in gBrowse (chr8:37821486..37821486 )