ADHDgene Database

SNP Report

Basic Info

Name	rs10491412 dbSNP Ensembl
Location	Chr5:50671121(Fwd)
Variant Alleles	C/T
Ancestral Allele	C
Functional Annotation	downstream_gene_variant; nc_transcript_variant; non_coding_exon_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000558403; ENST00000559112) nc_transcript_variant(ENST00000601500) non_coding_exon_variant(ENST00000601500)
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(a)	C/T		P-value=0.438 in the catergorical analysis, P-value>0.05 in ...... P-value=0.438 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: 1)

Approved Symbol	Approved Name	Location	No. of Studies (significant/non-significant/trend)
ISL1	ISL LIM homeobox 1	5q11.2	1(0/1/0)

SNPs in LD with rs10491412 (count: 1) View in gBrowse (chr5:50492629..50671121 )

The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r²>=0.8.