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	rs1799913 dbSNP Ensembl
Location	Chr11:18047255(Fwd)
Variant Alleles	G/T
Ancestral Allele	T
Functional Annotation	NMD_transcript_variant; downstream_gene_variant; intron_variant; splice_region_variant; upstream_gene_variant.
Consequence to Transcript	NMD_transcript_variant(ENST00000417164) downstream_gene_variant(ENST00000528338) intron_variant(ENST00000417164; ENST00000250018; ENST00000341556) splice_region_variant(ENST00000417164; ENST00000250018; ENST00000341556) upstream_gene_variant(ENST00000525406; ENST00000525523)
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
Johansson S, 2010			logistic regression P-value=0.39, OR=1.08 logistic regression P-value=0.39, OR=1.08	no significant association no significant association	Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources (count: 0)

SNPs in LD with rs1799913 (count: 0) View in gBrowse (chr11:18047255..18047255 )