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	rs2032893 dbSNP Ensembl
Location	chr5:36698622(Fwd)
Variant Alleles	C/T
Ancestral Allele	T
Functional Annotation	downstream_gene_variant; intron_variant; nc_transcript_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000508745; ENST00000512329) intron_variant(ENST00000510740) nc_transcript_variant(ENST00000510740)
No. of Studies	2 (significant: 0; non-significant: 2; trend: 0)
Source	Literature-origin

SNP related studies (count: 2)

Reference	Allele Change	Risk Allele	Statistical Values	Author Comments	Result of Statistical Analysis
Turic D, 2005(a)	A/G		allelic TRANSMIT P-value=0.05, X²=3.71 allelic TRANSMIT P-value=0.05, X²=3.71	produced modest evidence for association, with an excess of ...... produced modest evidence for association, with an excess of transmissions of allele G More...	Non-significant
Laurin N, 2008(a)	C/T		P-value=0.746 in the catergorical analysis, P-value>0.05 in ...... P-value=0.746 in the catergorical analysis, P-value>0.05 in the quantitative analysis More...	no significant evidence of association no significant evidence of association	Non-significant

SNP related genes (count: 0)

SNPs in LD with rs2032893 (count: 0) View in gBrowse (chr5:36698622..36698622 )