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	rs56164415 dbSNP Ensembl
Location	Chr11:27721735(Fwd)
Variant Alleles	G/A
Ancestral Allele	G
Functional Annotation	5_prime_UTR_variant; NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant.
Consequence to Transcript	5_prime_UTR_variant(ENST00000356660; ENST00000533246; ENST00000418212) NMD_transcript_variant(ENST00000530786) downstream_gene_variant(ENST00000502161; ENST00000500662; ENST00000499568) intron_variant(ENST00000395983; ENST00000438929; ENST00000530786; ENST00000525950; ENST00000532997; ENST00000395978; ENST00000395981; ENST00000584049; ENST00000530861; ENST00000530663; ENST00000420794; ENST00000314915; ENST00000395980) nc_transcript_variant(ENST00000584049; ENST00000530663) upstream_gene_variant(ENST00000395986; ENST00000533131)
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
Forero DA, 2009	C/T			Not significant for the total samples. Not significant for the total samples.	Non-significant

SNP related genes (count: 2)

Literature-origin genes (count: 1)

Genes from other sources (count: 1)

SNPs in LD with rs56164415 (count: 0) View in gBrowse (chr11:27721735..27721735 )