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	rs2075507 dbSNP Ensembl
Location	Chr22:19928092(Fwd)
Variant Alleles	G/A
Ancestral Allele	A
Functional Annotation	intron_variant; nc_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000400521; ENST00000400519; ENST00000400525; ENST00000474308; ENST00000334363; ENST00000535882; ENST00000496729) nc_transcript_variant(ENST00000474308; ENST00000496729) upstream_gene_variant(ENST00000361682; ENST00000467943; ENST00000407537; ENST00000403710; ENST00000403184)
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
Michaelovsky E, 2008	A/G		P-value=0.045, X²(1)=4.04 P-value=0.045, X²(1)=4.04	showed significant association with ADHD showed significant association with ADHD	Significant

SNP related genes (count: 2)

Literature-origin genes (count: 1)

Genes from other sources (count: 1)

SNPs in LD with rs2075507 (count: 0) View in gBrowse (chr22:19928092..19928092 )