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	rs17641078 dbSNP Ensembl
Location	chr9:1056959(Fwd)
Variant Alleles	G/C
Ancestral Allele	G
Functional Annotation	3_prime_UTR_variant; downstream_gene_variant; missense_variant. Polyphen Annotation: possibly damaging(ENST00000302441; ENST00000358146; ENST00000382251) SIFT Annotation: deleterious(ENST00000302441; ENST00000358146; ENST00000382251)
Consequence to Transcript	3_prime_UTR_variant(ENST00000259622; ENST00000382255) downstream_gene_variant(ENST00000412350) missense_variant(ENST00000302441; ENST00000358146; ENST00000382251)
No. of Studies	1 (significant: 0; non-significant: 0; trend: 1)
Source	Literature-origin

SNP related studies (count: 1)

Reference	Allele Change	Risk Allele	Statistical Values	Author Comments	Result of Statistical Analysis
Lasky-Su J, 2008			P-value=4.73E-06 under Additive model for FBAT-PC HI symptom...... P-value=4.73E-06 under Additive model for FBAT-PC HI symptoms; P-value=8.44E-06 under Dominant model for FBAT-PC HI symptoms More...	association finding with P-value association finding with P-value	Trend

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources (count: 0)

SNPs in LD with rs17641078 (count: 0) View in gBrowse (chr9:1056959..1056959 )