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	rs930072 dbSNP Ensembl
Location	Chr5:36666071(Fwd)
Variant Alleles	C/T
Ancestral Allele	C
Functional Annotation	downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000510740) intron_variant(ENST00000514563; ENST00000265113; ENST00000509272; ENST00000381918; ENST00000427100) nc_transcript_variant(ENST00000514563; ENST00000509272) upstream_gene_variant(ENST00000505376)
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
Turic D, 2005(a)	C/T		P-value=0.69 for pooled genotyping P-value=0.69 for pooled genotyping	not significantly associated with ADHD not significantly associated with ADHD	Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources (count: 0)

SNPs in LD with rs930072 (count: 0) View in gBrowse (chr5:36666071..36666071 )