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	rs1786581 dbSNP Ensembl
Location	Chr18:11852182(Fwd)
Variant Alleles	C/T
Ancestral Allele	C
Functional Annotation	3_prime_UTR_variant; intron_variant; nc_transcript_variant; upstream_gene_variant.
Consequence to Transcript	3_prime_UTR_variant(ENST00000526991) intron_variant(ENST00000269162; ENST00000334049; ENST00000585642; ENST00000535121; ENST00000423027; ENST00000590228; ENST00000586474) nc_transcript_variant(ENST00000586474) upstream_gene_variant(ENST00000588284)
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)	C/T		TDT P-value=0.384, X²=0.758 TDT P-value=0.384, X²=0.758	no significant evidence of association no significant evidence of association	Non-significant

SNP related genes (count: 2)

Literature-origin genes (count: 1)

Genes from other sources (count: 1)

SNPs in LD with rs1786581 (count: 0) View in gBrowse (chr18:11852182..11852182 )