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	rs1569061 dbSNP Ensembl
Location	Chr7:73114481(Fwd)
Variant Alleles	C/T
Ancestral Allele	C
Functional Annotation	3_prime_UTR_variant; NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant.
Consequence to Transcript	3_prime_UTR_variant(ENST00000222812; ENST00000395156) NMD_transcript_variant(ENST00000436944) downstream_gene_variant(ENST00000470878; ENST00000461441; ENST00000491427; ENST00000395154; ENST00000423497; ENST00000463307; ENST00000496216; ENST00000430446; ENST00000442099; ENST00000462135; ENST00000491645; ENST00000497980; ENST00000453316; ENST00000494245; ENST00000430270; ENST00000395155; ENST00000471215; ENST00000480126; ENST00000421744; ENST00000265758) intron_variant(ENST00000423166; ENST00000436944) nc_transcript_variant(ENST00000484736) non_coding_exon_variant(ENST00000484736)
No. of Studies	1 (significant: 1; non-significant: 0; trend: 0)
Source	Literature-origin

SNP related studies (count: 1)

Reference	Allele Change	Risk Allele	Statistical Values	Author Comments	Result of Statistical Analysis
Brookes KJ, 2005 (b)			MRM P-value=0.75, Case-control P-value=0.24, TDT P-value=0.0...... MRM P-value=0.75, Case-control P-value=0.24, TDT P-value=0.04 More...	was not significant in case-control analysis, but showed nom...... was not significant in case-control analysis, but showed nominal significance in TDT analysis More...	Significant

SNP related genes (count: 2)

Literature-origin genes (count: 1)

Genes from other sources (count: 1)

SNPs in LD with rs1569061 (count: 0) View in gBrowse (chr7:73114481..73114481 )