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	rs362986 dbSNP Ensembl
Location	Chr20:10277034(Fwd)
Variant Alleles	T/C
Ancestral Allele	T
Functional Annotation	downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000430336) intron_variant(ENST00000421143; ENST00000254976; ENST00000304886; ENST00000453544) nc_transcript_variant(ENST00000421143; ENST00000453544; ENST00000495883) non_coding_exon_variant(ENST00000495883)
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
Feng Y, 2005(b)	T/C		allelic TDT P-value=0.336, X²=0.925 in Irvine sam...... allelic TDT P-value=0.336, X²=0.925 in Irvine sample; allelic TDT P-value=0.112, X²=2.532 in Toronto sample More...	there was no significant result both in the Toronto sample a...... there was no significant result both in the Toronto sample and the Irvine sample More...	Non-significant

SNP related genes (count: 2)

Literature-origin genes (count: 1)

Genes from other sources (count: 1)

SNPs in LD with rs362986 (count: 0) View in gBrowse (chr20:10277034..10277034 )