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	rs60593443 dbSNP Ensembl
Location	Chr8:26636906(Fwd)
Variant Alleles	T/A
Ancestral Allele	T
Functional Annotation	NMD_transcript_variant; intron_variant; missense_variant; nc_transcript_variant.
Consequence to Transcript	NMD_transcript_variant(ENST00000519096; ENST00000521711) intron_variant(ENST00000354550; ENST00000276393; ENST00000380582; ENST00000519229; ENST00000380573; ENST00000521711; ENST00000380586; ENST00000519096; ENST00000518621; ENST00000380587; ENST00000380581) missense_variant(ENST00000380572) nc_transcript_variant(ENST00000518621)
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
Hawi, Z., 2012	T:A	T	P-value=0.1129, X²=2.51, OR=1.35, 95% CI=0.93-1.9...... P-value=0.1129, X²=2.51, OR=1.35, 95% CI=0.93-1.94 More...	The marker did not show significant association with ADHD. The marker did not show significant association with ADHD.	Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources (count: 0)

SNPs in LD with rs60593443 (count: 0) View in gBrowse (chr8:26636906..26636906 )