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	rs3787141 dbSNP Ensembl
Location	chr20:61989394(Fwd)
Variant Alleles	T/C
Ancestral Allele	C
Functional Annotation	intron_variant; nc_transcript_variant; NMD_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000370263; ENST00000463705; ENST00000467563; ENST00000498043) nc_transcript_variant(ENST00000463705; ENST00000467563) NMD_transcript_variant(ENST00000498043) upstream_gene_variant(ENST00000370257)
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
Lee J, 2008	T/C		P-value=0.166, X² (1df)=1.921 in all subtypes; P-...... P-value=0.166, X² (1df)=1.921 in all subtypes; P-value=0.439, X² (1df)=0.6 in inattentive subtype; P-value=0.046, X² (1df)=4 in combined subtype; P-value=0.044 in FBAT analysis for hyperactive/impulsive symptoms More...	nominally significant evidence of association with the ADHD ...... nominally significant evidence of association with the ADHD combined subtype and with teacher-rated hyperactivity- impulsivity scores More...	Significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources (count: 0)

SNPs in LD with rs3787141 (count: 0) View in gBrowse (chr20:61989394..61989394 )