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	rs6108464 dbSNP Ensembl
Location	Chr20:10283950(Fwd)
Variant Alleles	T/C
Ancestral Allele	T
Functional Annotation	intron_variant; nc_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000254976; ENST00000421143; ENST00000453544; ENST00000495883; ENST00000304886) nc_transcript_variant(ENST00000421143; ENST00000453544; ENST00000495883)
No. of Studies	2 (significant: 1; non-significant: 1; trend: 0)
Source	Literature-origin

SNP related studies (count: 2)

Reference	Allele Change	Risk Allele	Statistical Values	Author Comments	Result of Statistical Analysis
Guan L, 2009			single SNP association analyses: Nominal P-value=0.007, Empi...... single SNP association analyses: Nominal P-value=0.007, Empirical P-value=0.151 for ADHD; Nominal P-value=0.003, Empirical P-value=0.066 for ADHD-C More...	achieve nominal significance for ADHD and ADHD-C, also empir...... achieve nominal significance for ADHD and ADHD-C, also empirical significante for ADHD-C More...	Significant
Kim JW, 2007	T/C	C	Single marker analysis FBAT P-value=0.1; Exploratory analyse...... Single marker analysis FBAT P-value=0.1; Exploratory analyses FBAT P-value=0.257 for co-morbid CD, P-value=0.117 for co-morbid MDD, P-value=0.388 for co-morbid BD More...	No association was found between ADHD or co-morbidities of A...... No association was found between ADHD or co-morbidities of ADHD and this SNP More...	Non-significant

SNP related genes (count: 2)

Literature-origin genes (count: 1)

Genes from other sources (count: 1)

SNPs in LD with rs6108464 (count: 0) View in gBrowse (chr20:10283950..10283950 )