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	rs787558 dbSNP Ensembl
Location	Chr18:11865878(Fwd)
Variant Alleles	C/T
Ancestral Allele	C
Functional Annotation	intron_variant; nc_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000334049; ENST00000535121; ENST00000590228; ENST00000585642; ENST00000269162; ENST00000535980; ENST00000423027) nc_transcript_variant(ENST00000535980)
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
Laurin N, 2008(b)	T/C		TDT P-value=0.363, X²=0.828 TDT P-value=0.363, X²=0.828	no significant evidence of association no significant evidence of association	Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources (count: 0)

SNPs in LD with rs787558 (count: 0) View in gBrowse (chr18:11865878..11865878 )