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	rs4860 dbSNP Ensembl
Location	Chr12:63359783(Fwd); Chr3:40503754(Fwd)
Variant Alleles	T/C
Ancestral Allele	T
Functional Annotation	3_prime_UTR_variant; downstream_gene_variant; nc_transcript_variant; non_coding_exon_variant.
Consequence to Transcript	3_prime_UTR_variant(ENST00000338970; ENST00000416518; ENST00000396203) downstream_gene_variant(ENST00000435633; ENST00000461368; ENST00000465280; ENST00000481798; ENST00000465325; ENST00000484568; ENST00000266610) nc_transcript_variant(ENST00000479563) non_coding_exon_variant(ENST00000479563)
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
Wang G. X., 2012	A/G	A	Chi-square test: genotypic p>0.05; allelic p>0.05 Chi-square test: genotypic p>0.05; allelic p>0.05	The genotype distribution and allele frequencies of this SNP...... The genotype distribution and allele frequencies of this SNP showed no significant difference between ADHD children and healthy controls. More...	Non-significant

SNP related genes (count: 3)

Literature-origin genes (count: 1)

Genes from other sources (count: 2)

SNPs in LD with rs4860 (count: 0) View in gBrowse (chr12; 3:63359783..63359783 )