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	rs498793 dbSNP Ensembl
Location	Chr11:61624705(Fwd)
Variant Alleles	T/C
Ancestral Allele	T
Functional Annotation	intron_variant; nc_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000257261; ENST00000522056; ENST00000278840; ENST00000523235; ENST00000521571; ENST00000355484; ENST00000521849) nc_transcript_variant(ENST00000523235) upstream_gene_variant(ENST00000522359)
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
Brookes KJ, 2006(a)	C/T		allelic P-value=0.0037, OR=1.6; TDT P-value=0.013, OR=1.69 (...... allelic P-value=0.0037, OR=1.6; TDT P-value=0.013, OR=1.69 (C allele), OR=0.53 (T allele); HHRR P-value=0.018, OR=1.2 (C allele), OR=0.75 (T allele) More...	significant association with ADHD was detected in both case-...... significant association with ADHD was detected in both case-control and within-family analyses More...	Significant
Brookes K, 2006	A/G		UNPHASED TDT P-value=0.45; WHAP TDT P-value=0.116 UNPHASED TDT P-value=0.45; WHAP TDT P-value=0.116	no significant association was observed no significant association was observed	Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources (count: 0)

SNPs in LD with rs498793 (count: 0) View in gBrowse (chr11:61624705..61624705 )